With ongoing and ground-breaking developments in Oncology and Rare Disease, an increased focus on more scientific, targeted medicine and continuous integration of technology into development and delivery of medicine, there has never been a more exciting time to join us!
As a global leader we're looking for a Senior **Lead Clinical Research Associate (CRA)** to drive success as part of our Non-interventional Study team.
Join Oracle as a Lead CRA and make a real impact by guiding teams, ensuring top-quality clinical research, and driving groundbreaking projects on a global scale!
**What you will do**
**As a Senior Lead Clinical Research Associate at Oracle, you will:**
+ **Drive study start-up:** Develop feasibility questionnaires, identify and assess potential study sites, and ensure proper site selection in close collaboration with Project Managers and Sponsors.
+ **Oversee contracts and budgets:** Review and track site contracts and budgets for study specifications, working closely with CRA and contracting teams, and involve contract specialists for legal matters.
+ **Ensure regulatory compliance:** Coordinate with regulatory teams and CRAs to ensure all ethical committee (EC) requirements are met and support the preparation and submission of essential site documents.
+ **Lead study site management:** Supervise site activation and ongoing management, including monitoring activities from feasibility to close-out, in line with GCP, SOPs, study protocols, and plans.
+ **Train and coordinate CRAs:** Oversee, mentor, and train a cross-country team of Clinical Research Associates, develop project-specific training materials, and ensure delivery of high-quality site management.
+ **Monitor progress and quality:** Create and maintain study trackers, monitor CRA activities and site deliverables, identify and escalate critical issues, and review/approve monitoring reports.
+ **Foster team collaboration:** Act as the key point of contact between the study team, Sponsor, study sites, and CRAs, supporting strong working relationships and continuous process improvement.
+ **Travel for site initiations, closures or quality visits:** Be available to travel to clinical sites to train and monitor site activities as needed. While there is no guaranteed travel, flexibility is required.
**Required Experience**
+ **Education** : Bachelor's degree in Life Sciences, Medical Science, Pharmacy, Public Health, or equivalent, with a minimum of three years' hands-on clinical research experience.
+ **Clinical research expertise** : At least 3 years of experience as a CRA, including site initiation, Trial Master File (TMF) management, and site monitoring for both clinical and non-interventional studies.
+ **Communication skills** : Outstanding spoken and written proficiency in English (C1 level minimum).Additional languages are considered a strong asset.
+ **Technical proficiency** : Comfort with MS Office, EDC, CTMS exprience and willingness to learn and handle various technical systems and tools.
+ **Personal qualities** : Exceptional organizational and problem-solving skills, strong cross-culturalteamwork, initiative in process optimization, and the ability to manage competing priorities in a fast-paced environment.
+ **Financial management:** Experience reviewing site contracts, budget and invoices.
+ **Attention to detail** : Ability to work independently with careful, precise, and thorough execution of complex tasks.
**Responsibilities**
**What you will do**
**As a Senior Lead Clinical Research Associate at Oracle, you will:**
+ **Drive study start-up:** Develop feasibility questionnaires, identify and assess potential study sites, and ensure proper site selection in close collaboration with Project Managers and Sponsors.
+ **Oversee contracts and budgets:** Review and track site contracts and budgets for study specifications, working closely with CRA and contracting teams, and involve contract specialists for legal matters.
+ **Ensure regulatory compliance:** Coordinate with regulatory teams and CRAs to ensure all ethical committee (EC) requirements are met and support the preparation and submission of essential site documents.
+ **Lead study site management:** Supervise site activation and ongoing management, including monitoring activities from feasibility to close-out, in line with GCP, SOPs, study protocols, and plans.
+ **Train and coordinate CRAs:** Oversee, mentor, and train a cross-country team of Clinical Research Associates, develop project-specific training materials, and ensure delivery of high-quality site management.
+ **Monitor progress and quality:** Create and maintain study trackers, monitor CRA activities and site deliverables, identify and escalate critical issues, and review/approve monitoring reports.
+ **Foster team collaboration:** Act as the key point of contact between the study team, Sponsor, study sites, and CRAs, supporting strong working relationships and continuous process improvement.
+ **Travel for site initiations, closures or quality visits:** Be available to travel to clinical sites to train and monitor site activities as needed. While there is no guaranteed travel, flexibility is required.
Disclaimer:
**Certain US customer or client-facing roles may be required to comply with applicable requirements, such as immunization and occupational health mandates.**
**Range and benefit information provided in this posting are specific to the stated locations only**
US: Hiring Range in USD from: $70,600 to $141,200 per annum. May be eligible for bonus and equity.
Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business.
Candidates are typically placed into the range based on the preceding factors as well as internal peer equity.
Oracle US offers a comprehensive benefits package which includes the following:
1. Medical, dental, and vision insurance, including expert medical opinion
2. Short term disability and long term disability
3. Life insurance and AD&D
4. Supplemental life insurance (Employee/Spouse/Child)
5. Health care and dependent care Flexible Spending Accounts
6. Pre-tax commuter and parking benefits
7. 401(k) Savings and Investment Plan with company match
8. Paid time off: Flexible Vacation is provided to all eligible employees assigned to a salaried (non-overtime eligible) position. Accrued Vacation is provided to all other employees eligible for vacation benefits. For employees working at least 35 hours per week, the vacation accrual rate is 13 days annually for the first three years of employment and 18 days annually for subsequent years of employment. Vacation accrual is prorated for employees working between 20 and 34 hours per week. Employees working fewer than 20 hours per week are not eligible for vacation.
9. 11 paid holidays
10. Paid sick leave: 72 hours of paid sick leave upon date of hire. Refreshes each calendar year. Unused balance will carry over each year up to a maximum cap of 112 hours.
11. Paid parental leave
12. Adoption assistance
13. Employee Stock Purchase Plan
14. Financial planning and group legal
15. Voluntary benefits including auto, homeowner and pet insurance
The role will generally accept applications for at least three calendar days from the posting date or as long as the job remains posted.
Career Level - IC3
**About Us**
As a world leader in cloud solutions, Oracle uses tomorrow's technology to tackle today's challenges. We've partnered with industry-leaders in almost every sector-and continue to thrive after 40+ years of change by operating with integrity.
We know that true innovation starts when everyone is empowered to contribute. That's why we're committed to growing an inclusive workforce that promotes opportunities for all.
Oracle careers open the door to global opportunities where work-life balance flourishes. We offer competitive benefits based on parity and consistency and support our people with flexible medical, life insurance, and retirement options. We also encourage employees to give back to their communities through our volunteer programs.
We're committed to including people with disabilities at all stages of the employment process. If you require accessibility assistance or accommodation for a disability at any point, let us know by emailing accommodation-request_************* or by calling *************** in the United States.
Oracle is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans' status, or any other characteristic protected by law. Oracle will consider for employment qualified applicants with arrest and conviction records pursuant to applicable law.
$70.6k-141.2k yearly 4d ago
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Research Compliance Administrator (Pooled Posting)
Auburn University 3.9
Clinical coordinator job in Auburn, AL
Details Information Requisition Number S4591P Home Org Name Office of Research Compliance Division Name VP for Research and Economic Dev Position Title Research Compliance Administrator (Pooled Posting) Job Class Code HC80 Appointment Status Full-time Part-time FTE Limited Term No Limited Term Length Job Summary
This is a pooled posting. This posting will remain open for an extended period of time and selected applicants will be contacted as future staffing needs arise.
Auburn University's Office of the Sr. Vice President of Research and Economic Development is accepting applications for the position of Research Compliance Administrator. This position contributes to the daily activities of the Research Compliance Program(s) within the Office of Research Compliance (ORC), which includes the Animal Care and Use Program, the Human Research Protection Program, and the Biological Safety Program. This role ensures adherence to federal and state regulations, sponsor-specific requirements, and institutional policies, and its efforts are essential in maintaining the integrity and ethical standards of our research initiatives.
Essential Functions
* Organizes, coordinates, and executes daily activities of the research compliance programs to ensure adherence to regulatory, contractual, and policy requirements.
* Reviews and assists with research protocols, guiding investigators, faculty, and staff through the protocol submission process to ensure compliance.
* Provides subject-matter advice and oversight on non-compliance assessments, inquiries, investigations, audits, and inspections, including preparing necessary reports and follow-ups.
* Develops, reviews, and revises compliance policies, procedures, and guidelines, enhancing institutional and departmental strategies. Establishes goals and objectives to identify successful program indicators.
* Supports accreditation efforts by preparing and submitting annual/interim reports, coordinating re-accreditation materials, and ensuring compliance with accreditation standards.
* Develops and implements educational programs to promote compliance and responsible conduct of research, including conducting training sessions, seminars, and workshops.
* Remains current on regulatory requirements and organizational demands by attending workshops and seminars and disseminates relevant information as needed.
* Performs additional duties as assigned to support the overall mission of the research compliance programs.
Why Work at Auburn?
* Life-Changing Impact: Our work changes lives through research, instruction, and outreach, making a lasting impact on our students, our communities, and the world.
* Culture of Excellence: We are committed to leveraging our strengths, resources, collaboration, and innovation as a top employer in higher education.
* We're Here for You: Auburn offers generous benefits, educational opportunities, and a culture of support and work/life balance.
* Sweet Home Alabama: The Auburn/Opelika area offers southern charm, vibrant downtown scenes, top-ranked schools, and easy access to Atlanta, Birmingham, and the Gulf of Mexico beaches.
* A Place for Everyone: Auburn is committed to fostering an environment where all faculty, staff, and students are welcomed, valued, respected, and engaged.
Ready to lead and shape the future of higher education? Apply today! War Eagle!
Minimum Qualifications
Minimum Qualifications
* Bachelor's degree- No specific discipline
* 4 years of Contracts and Grants, Compliance, Research, Research Administration, or other related experience.
Minimum Skills, License, and Certifications
Minimum Skills and Abilities
Strong organizational, administrative, communication, and interpersonal skills. |
Proficient computer skills with Internet and MS Office (Outlook, Word, Excel etc.).
Minimum Technology Skills Minimum License and Certifications
Desired Qualifications
Desired Qualifications
* Higher Education experience
* Master's degree
* Knowledge of federal regulations, state laws, and institutional policies and procedures related to animal care and use, human subject research protection, or biological hazards required based on program assignment.
Posting Detail Information
Salary Range $49,220-$83,680 Job Category Research Working Hours if Non-Traditional City position is located in: Auburn State position is located: AL List any hazardous conditions or physical demands required by this position Posting Date 07/16/2025 Closing Date Equal Opportunity Compliance Statement
It is our policy to provide equal employment and education opportunities for all individuals without regard to race, color, national origin, religion, sex, sexual orientation, gender identity, gender expression, pregnancy, age, disability, protected veteran status, genetic information, or any other classification protected by applicable law. Please visit their website to learn more.
Special Instructions to Applicants Quick Link for Internal Postings *******************************************
Documents Needed to Apply
Required Documents
* Resume
* Cover Letter
Optional Documents
Supplemental Questions
Required fields are indicated with an asterisk (*).
* * Please tell us how you first heard about this opportunity.
(Open Ended Question)
* * Please select the answer that best describes your current employment relationship with Auburn University:
* Current full-time Auburn or AUM employee within probationary period
* Current full-time Auburn or AUM employee outside of probationary period
* Current part-time Auburn or AUM employee
* Not an Auburn or AUM employee
* * Do you have a Bachelor's degree from an accredited institution?
* Yes
* No
* * Do you have 4 years of contracts and grants, compliance, research, research administration, or other related experience?
* Yes
* No
$49.2k-83.7k yearly 14d ago
Trial Master File (TMF) Specialist Oncology
Sumitomo Pharma 4.6
Clinical coordinator job in Montgomery, AL
Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website ********************************** or follow us on LinkedIn.
The Trial Master File (TMF) Specialist will be responsible for ensuring that SMPA studies have comprehensive and quality Trial Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable functions follow the requirements of the TMF SOP and system work instructions. Provide support and guidance to study team members during the full lifecycle of the study, including planning, set-up, maintenance, QC and closure of the study TMF.
**Key Responsibilities**
+ Responsible for overall quality, maintenance, and completeness of Trial Master Files.
+ Working closely with the TMF Process Owner, identify trends or quality concerns and oversee resolution of issues.
+ Develop project specific TMF plan and structure and update the plan as needed.
+ Participate in system UAT as needed and collaborate with Information Technology to ensure system validation is maintained.
+ Work closely with Clinical Operations and Regulatory Affairs to ensure compliance with regulatory requirements.
+ Act as a liaison between the Site IRBs and study team to resolve queries and concerns.
+ Provide study team reports or updates regarding status of TMF on a regular basis.
+ Participate in audits and provide documents as requested.
+ Perform investigation of deviations and monitoring of Corrective actions & preventive actions (CAPA) relating to non-compliance issues and findings.
+ Oversee TMF maintenance done by CROs and ensure final transfer of TMF is sufficient to support any potential regulatory filings.
+ Champion best practices for building and maintaining TMF health.
**Professional Experience / Qualifications**
+ BA/BS with minimum of 3 year of clinical research experience in academic and/or industry settings
+ Knowledge of and direct experience with Trial Master Files.
+ Prior eTMF (e.g. Veeva) administration required.
+ Strong Microsoft Office skills required.
+ Demonstrate a comprehensive knowledge of Good Clinical Practice, Good Documentation Practice, and International Council for Harmonization E6(R2).
+ Fundamental knowledge of the conduct of clinical trials is preferred.
+ Strong focus on teamwork, attention to detail, excellent organizational skills. Must have ability to prioritize, and the ability to work in a multi-task environment.
The base salary range for this role is $72,500 to $90,600. Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state. Our robust time-off policy includes flexible paid time off, 11 paid holidays plus additional time off for a shut-down period during the last week of December, 80 hours of paid sick time upon hire and each year thereafter. Total compensation, including base salary to be offered, will depend on elements unique to each candidate, including candidate experience, skills, education and other factors permitted by law.
Disclaimer: The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed.
**Confidential Data** : All information (written, verbal, electronic, etc.) that an employee encounters is considered confidential.
**Compliance** : Achieve and maintain Compliance with all applicable regulatory, legal and operational rules and procedures, by ensuring that all plans and activities for and on behalf of Sumitomo Pharma America (SMPA) and affiliates are carried out with the "best" industry practices and the highest ethical standards.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
**Mental/Physical Requirements** : Fast paced environment handling multiple demands. Must be able to exercise appropriate judgment as necessary. Requires a high level of initiative and independence. Excellent written and oral communication skills required. Requires ability to use a personal computer for extended periods of time.
**Sumitomo Pharma America (SMPA)** **is an Equal Employment Opportunity (EEO) employer**
Qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website ********************************** or follow us on LinkedIn.
Sumitomo Pharma America (SMPA) endeavors to make its application process accessible to all. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact SMPA at **********************************************
This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.
At Sumitomo Pharma America, our work is guided by the Sumitomo Pharma mission, vision and values, which tie closely to our company's cultural pillars.
**Our** **Mission**
_To broadly contribute to society through value creation based on innovative research and development activities for the betterment of healthcare and fuller lives of people_ _worldwide_
**Our** **Vision**
_For Longer and Healthier Lives, we unlock the future with cutting edge technology and_ _ideas_
$72.5k-90.6k yearly 60d+ ago
Sr. Clinical Research Associate - FSP
Parexel 4.5
Clinical coordinator job in Montgomery, AL
**CRA and Sr CRA positions- Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficient manner. The CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery of the study.
The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with Client Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.
**Key Accountabilities** :
**Site Management Responsibilities**
+ Contributes to the selection of potential investigators.
+ In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance. Tasks may include Site Qualification Visits, collection, preparation, review and tracking of documents for the application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start-up and for the duration of the study.
+ Trains, supports, and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles.
+ Confirms that site staff have completed and documented the required training appropriately, including ICH-GCP training, prior to and for the duration of the study. Ensures the sites are inspection ready at all times.
+ Actively participates in Local Study Team (LST) meetings.
+ Contributes to National Investigators meetings, as applicable.
+ Initiates, monitors, and closes study sites in compliance with Client Procedural Documents. Shares information on patient recruitment and study site progress (site quality/performance) within the LST.
+ Drives performance at the sites. Proactively identifies and ensures timely resolution to study-related issues and escalates them as appropriate.
+ Updates CTMS and other systems with data from study sites as per required timelines.
+ Manages study supplies (Investigator Site File (ISF), etc.), drug supplies and drug accountability at study site. Prepares study drug for destruction, if applicable.
+ Performs monitoring visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Monitoring Plan. If required, determines, and discusses with LSAD the correct timing and type of visits.
+ Performs Source Data Review (SDR), Case Report Form (CRF) review and Source Data Verification (SDV), in accordance with the Monitoring Plan.
+ Performs regular Site Quality Risk Assessments and adapts monitoring intensity accordingly during the study.
+ Ensures data query resolution in a timely manner.
+ Works with data management to ensure robust quality of the collected study data.
+ Ensures accurate and timely reporting of Serious Adverse Events and their follow ups.
+ Prepares and finalizes monitoring visit reports in CTMS and provides timely feedback to the Principal Investigator, including follow-up letter, within required timelines and in line with Client SOP.
+ Follows up on outstanding actions with study sites to ensure resolution in a timely manner.
+ Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required.
+ Assists site in maintaining inspection ready ISF.
+ Prepares for and collaborates with the activities associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD).
+ Ensures timely collection/uploading of essential documents into the eTMF in accordance with ICH-GCP, Client SOPs and local requirements. Supports/participates in regular QC checks performed by LSAD or delegate.
+ Ensures that all study documents under their responsibility (i.e., site documents, relevant communications, etc.) are available and ready for final archiving and completion of local part of the eTMF.
+ Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market.
+ Collaborates with local Medical Science Liaisons (MSLs) as directed by LSAD or line manager.
**Compliance with Sponsor Standards**
+ Ensures compliance with the Client's Code of Ethics and company policies and procedures relating to people, finance, technology, security, and SHE (Safety, Health and Environment).
+ Ensures compliance with local, national, and regional legislation, as applicable.
+ Completes timesheets accurately as required.
**Compliance with Parexel Standards**
+ Complies with required training curriculum.
+ Completes timesheets accurately as required.
+ Submits expense reports as required.
+ Updates CV as required.
+ Maintains working knowledge of and complies with Parexel/Client processes, ICH-GCPs and other applicable requirements.
**Skills (Essential):**
+ Excellent attention to detail.
+ Good written and verbal communication skills.
+ Good collaboration and interpersonal skills.
+ Good negotiation skills.
+ Proficient in written and spoken English language required.
+ Fluency in local language(s) required.
**Skills (Desirable):**
+ Ability to work in an environment of remote collaborators.
+ Manages change with a positive approach for self, team, and the business. Sees change as an opportunity to improve performance and add value to the business.
+ Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time.
+ Good analytical and problem-solving skills.
+ Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.
+ Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment.
+ Team oriented and flexible; ability to respond quickly to shifting demands and opportunities.
**Knowledge and Experience (Essential)** **:**
+ Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP.
+ Good knowledge of relevant local regulations.
+ Good medical knowledge and ability to learn relevant Client Therapeutic Areas.
+ Basic understanding of the drug development process.
+ Good understanding of Clinical Study Management including monitoring, study drug handling and data management.
**Knowledge and Experience (Desired):**
+ Familiar with risk-based monitoring approach including remote monitoring.
+ Good cultural awareness.
**Education:**
+ Bachelor's degree in related discipline, preferably in life science, or equivalent qualification (adapted to local country market needs), that supports skills and capabilities of the position and ensures successful conduct of responsibilities and appropriate interactions with internal and or external customers.
**Other:**
+ Ability to travel nationally/internationally as Required
+ Valid driving license per country requirements, as applicable.
LI-LG4
\#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
$75k-97k yearly est. 42d ago
Disability Clinical Specialist
Sedgwick 4.4
Clinical coordinator job in Montgomery, AL
By joining Sedgwick, you'll be part of something truly meaningful. It's what our 33,000 colleagues do every day for people around the world who are facing the unexpected. We invite you to grow your career with us, experience our caring culture, and enjoy work-life balance. Here, there's no limit to what you can achieve.
Newsweek Recognizes Sedgwick as America's Greatest Workplaces National Top Companies
Certified as a Great Place to Work
Fortune Best Workplaces in Financial Services & Insurance
Disability Clinical Specialist
**PRIMARY PURPOSE** : Performs standard clinical evaluations on claims that require additional review based on medical condition, client requirement, and/or complexity. Consults with providers and employees by providing case direction and ensures medical information substantiates the need for employee absence from work.
**ESSENTIAL FUNCTIONS and RESPONSIBILITIES**
+ Performs standard clinical reviews of referred medical claims based on client requirements to ensure accurate and sufficient information is received by employees and providers to support the claim request and documents decision rationale.
+ Completes medical review of all claims by reviewing medical documentation received and applying practical clinical knowledge to ensure information substantiates disability and to interpret the impact the condition has on the ability to perform job functions.
+ Communicates clearly and professionally, on the phone and/or in writing with employee and/or providers to discuss employee's clinical status, progress, and work status.
+ Provides clear and appropriate follow-up recommendations for ongoing medical management of claims; ensures appropriate recommendations are made on claims.
+ Consistently achieves appropriate quality audit scores.
+ Acts as clinical resource to claims examiners to provide guidance on the medical management of claims including comprehension of medical terminology and substantiating claim decisions.
**ADDITIONAL FUNCTIONS and RESPONSIBILITIES**
+ Acts as a backup for key disability claims on an ad hoc basis.
+ Performs other duties as assigned.
+ Travels as required.
**QUALIFICATIONS**
**Education & Licensing**
Bachelor's degree or equivalent preferred. Current RN, CRC, LPC and/or LCSW Licenses required. Current license, registration and/or professional designations as required within the jurisdiction. Clinical expertise must be kept current by acquisition of the necessary CEUs to maintain licenses and designations.
**Experience**
Four (4) years of related experience or equivalent combination of experience and education required to include experience in a direct medical/psychological setting or physical industrial medicine and previous insurance or related experience.
**Skills & Knowledge**
+ Knowledge of current medical practices in health care management in a variety of areas (including, but not limited to, orthopedics, general medicine for acute and chronic conditions, general surgery, mental health, obstetrics, oncology, and physical and occupational rehabilitation)
+ Excellent oral and written communication, including presentation skills
+ Proficient computer skills including working knowledge of Microsoft Office
+ Analytical and interpretive skills
+ Strong organizational and multitasking skills
+ Excellent interpersonal skills
+ Ability to exercise judgement and critical thinking skills
+ Ability to work in a team environment
+ Ability to meet or exceed Performance Competencies
**WORK ENVIRONMENT**
When applicable and appropriate, consideration will be given to reasonable accommodations.
**Mental:** Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadlines
**Physical:** Ability to sit at a desk for extended periods while operating a computer and phone system. Travel as required.
**Auditory/Visual:** Hearing, vision and talking
Always accepting applications
The statements contained in this document are intended to describe the general nature and level of work being performed by a colleague assigned to this description. They are not intended to constitute a comprehensive list of functions, duties, or local variances. Management retains the discretion to add or to change the duties of the position at any time.
_As required by law, Sedgwick provides a reasonable range of compensation for roles that may be hired in jurisdictions requiring pay transparency in job postings. Actual compensation is influenced by a wide range of factors including but not limited to skill set, level of experience, and cost of specific location. For the jurisdiction noted in this job posting only, the range of starting pay for this role is_ _$62,000-$63,000 USD Annual_ _. A comprehensive benefits package is offered including but not limited to, medical, dental, vision, 401k and matching, PTO, disability and life insurance, employee assistance, flexible spending or health savings account, and other additional voluntary benefits._
Sedgwick is an Equal Opportunity Employer and a Drug-Free Workplace.
**If you're excited about this role but your experience doesn't align perfectly with every qualification in the job description, consider applying for it anyway! Sedgwick is building a diverse, equitable, and inclusive workplace and recognizes that each person possesses a unique combination of skills, knowledge, and experience. You may be just the right candidate for this or other roles.**
**Sedgwick is the world's leading risk and claims administration partner, which helps clients thrive by navigating the unexpected. The company's expertise, combined with the most advanced AI-enabled technology available, sets the standard for solutions in claims administration, loss adjusting, benefits administration, and product recall. With over 33,000 colleagues and 10,000 clients across 80 countries, Sedgwick provides unmatched perspective, caring that counts, and solutions for the rapidly changing and complex risk landscape. For more, see** **sedgwick.com**
The Associate Clinical Specialist independently provides customer support of Fujifilm's ES equipment in the Endoscopy department and/or specified departments. This role manages all relevant equipment and uses its own judgement and decision-making skills to provide troubleshooting and training for the proper handling of our equipment. This position provides on-site, hands-on client support for Fujifilm Endoscopy's entire product catalog for assigned customers. It serves as the primary clinical resource for the Company and its sales team regionally and handles all related inquiries and issues. The ACS partners with and provides training to all members of the customer's staff, including physicians, reprocessing department, technicians, and nurses to independently manage and maintain customers' Fujifilm equipment. Furthermore, it provides service to additional customers within the zone as required. This position reports directly to the Zone Sales Director or Regional Manager.
**Company Overview**
At FUJIFILM Healthcare Americas Corporation, we're on a mission to innovate for a healthier world, and we need passionate, driven people like you to help us get there. Our cutting-edge healthcare solutions span diagnostic imaging, enterprise imaging, endoscopic and surgical imaging, as well as in-vitro diagnostics.
But we don't stop at healthcare; our Non-Destructive Testing (NDT) team harnesses advanced radiography solutions to keep transportation infrastructure, aerospace, and oil and gas assets safe and running smoothly.
Ready to innovate, collaborate, and make a difference? Join us and bring your big ideas to life while working in a dynamic, flexible environment that fuels your creativity and drive.
Our headquarters is in Lexington, Massachusetts, an inspiring healthcare research hub in a historic town.
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: ***************************************************
**Job Description**
**Duties and Responsibilities:**
+ Serve as the primary resource by providing continuous training and education of Fujifilm's equipment and/or services for our regional based customers.
+ Deliver post sale, face-to-face client support which includes performing all associated responsibilities based upon the agreement with the account system which generally includes:
+ Set up and support Fujifilm video tower / system.
+ Inspect, troubleshoot, and maintain all Fujifilm equipment.
+ Monitor, report, and support repair transactions.
+ Provide Case observation, continuous staff training on Fujifilm technologies, and overall Fujifilm customer and technology support.
+ Provide daily maintenance and independent management of the client's Fujifilm equipment.Identify process improvement opportunities and design workflows to improve efficiency and reduce overall repairs using own judgement.
+ Serve as primary point of contact for understanding repair history, conducting root cause analysis to troubleshoot issues, and implementing plans to minimize repairs and prevent future handling damages.
+ Serve as a clinical liaison by developing and delivering comprehensive weekly and monthly reports to senior management that details installation and usage progress/metrics, staff training needs and effectiveness of completed training, and identifying trends to inform and strengthen KOL (Key Opinion Leader) relationships that support strategic decision making.
+ Analyze and present data-driven insights to monitor installation and usage progress, ensuring optimal staff training and identifying trends that influence strategic planning.
+ Provide and maintain customer data for integration into a future database application.
+ Attend local, regional, and national trade shows as requested.
+ Adhere to all safety policies and procedures.
+ Comply with all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable laws, regulations, and standards.
**Qualifications:**
+ High School Diploma or equivalent is required.
+ Bachelor's degree in business, marketing or related quantitative disciplines preferred.
+ Minimum of 2 years of field sales or clinical experience desired.
+ Knowledge of and experience in GI/pulmonary flexible endoscopy. Experience in advanced therapeutic procedures highly preferred.
+ Operate a computer effectively and efficiently, including being proficient in Microsoft Office (i.e. Word, Excel, and PowerPoint) and MS Outlook and other email applications.
+ Strong oral and written communication skills to relay technical information and to professionally communicate with internal and external customers and team members at all levels.
+ Ability to troubleshoot all Fujifilm endo equipment and determine root cause of issues.
+ Strong time management skills.
+ Decision-making skills to determine usage of FUJIFILM equipment and type of training needed by customers to effectively utilize the technology.
+ Ability to provide expert guidance, training, and support to ensure workflow optimization for Fujifilm and our customers.
+ Ability to analyze data to present data driven insights.
+ Ability to multi-task and work on several projects simultaneously.
+ Ability to prioritize customer requirements.
+ Ability to present information in front of small groups of people.
+ Ability to understand basic mathematical requirements for discount calculation.
Physical requirements:
+ The ability to use hands and fingers to feel and manipulate items, including keyboards.
+ The ability to stand, talk, and hear.
+ The ability to lift and carry up to 25-50 lbs.
+ Close Vision: The ability to see clearly at twenty inches or less.
Travel:
+ Travel requirements 50% of the time.
+ Full territory for this position includes Des Moines/Iowa. Travel to and service of the entire region is required and expected as part of the job responsibilities.
**Salary and Benefits:**
+ $59,000.00, $8,000 KPI, Company Car
+ Medical, Dental, Vision
+ Life Insurance
+ 401k
+ Paid Time Off
* \#LI-Remote
_In the event that COVID-19 vaccine mandates issued by the federal government, or by state or local government become effective and enforceable, the Company will require that the successful candidate hired for positions covered under relevant government vaccine mandate(s) be fully vaccinated against COVID-19, absent being granted an accommodation due to medical or sincerely held religious belief or other legally required exemption._
_Applicants to positions where vendor credentialing or other similar requirements exist to enter facilities will be required to comply with the credentialing requirements of the facilities, including complying with vaccine requirements._
_For all positions, the Company encourages vaccination against COVID-19 and requires that the successful candidate hired be willing to test for the COVID-19 virus periodically and wear a face covering indoors as required, absent being granted an accommodation due to medical or sincerely held religious belief or other legally required exemption._
**EEO Information**
Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.
**ADA Information**
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (****************************** or ***************.
**Job Locations** _US-Remote_
**Posted Date** _6 days ago_ _(1/13/2026 12:52 PM)_
**_Requisition ID_** _2025-36149_
**_Category_** _Clinical_
**_Company (Portal Searching)_** _FUJIFILM Healthcare Americas Corporation_
$59k yearly 35d ago
Care Coordinator Exempt - Eamc Case Mgmt
East Alabama Hospital 4.1
Clinical coordinator job in Opelika, AL
EAMC MISSION
At East Alabama Medical Center, our mission is high quality, compassionate health care, and that statement guides everything we do. We set high standards for customer service, quality, and keeping costs under control.
POSITION SUMMARY
Identifies and assesses patients in need of services to meet their medical, psychosocial and financial needs. Demonstrates fiscal responsibility through timely, efficient and appropriate discharges. Meets Department professional development standards Works as a team member to develop appropriate discharge plans through review of the medical record, conferences with other members of the healthcare team and patient care conferences.
POSITION QUALIFICATIONS
Minimum Education
Associate Degree RN or Bachelor of Social Work
Minimum Experience
2 years nursing or medical social work.
Required Registration/License/Certification
Active Alabama license by State Board of Social Work or Registered Nurse
Preferred Education
BSN or MSW
Preferred Experience
5 years nursing or social work experience in case management or medical social work
Preferred Registration/License/Certification
Case Management Certification from an Accredited Organization
Other Requirements
N/A
$52k-67k yearly est. 49d ago
Clinical Manager
Amedisys Inc. 4.7
Clinical coordinator job in Opelika, AL
Full Time Monday - Friday RN Home Health - 1 year required 1 year of Clinical Management required Are you looking for a rewarding career in homecare? If so, we invite you to join our team at Amedisys, one of the largest and most trusted home health and hospice companies in the U.S.
Attractive pay
$80,000.00 to $95,000.00 Annually
What's in it for you
* A full benefits package with choice of affordable PPO or HSA medical plans.
* Paid time off.
* Up to $1,000 in free healthcare services paid by Amedisys yearly, when enrolled in an Amedisys HSA medical plan.
* Up to $500 in wellness rewards for completing activities during the year. Use these rewards to support your wellbeing with spa services, gym memberships, sports, hobbies, pets and more.*
* Mental health support, including up to five free counseling sessions per year through the Amedisys Employee Assistance program.
* 401(k) with a company match.
* Family support with infertility treatment coverage*, adoption reimbursement, paid parental and family caregiver leave.
* Fleet vehicle program (restrictions apply) and mileage reimbursement.
* And more.
Please note: Benefit eligibility can vary by position depending on shift status.
* To participate, you must be enrolled in an Amedisys medical plan.
Why Amedisys?
* Community-based care centers with a supportive and inclusive work environment.
* Better work/life balance and increased flexibility compared to other settings.
* Job stability and the opportunity to advance with a growing company.
* The opportunity to make a meaningful impact on the lives of patients and their families providing much needed care where they want to be - in their homes.
Responsibilities
* Recommends employment decisions for staff to the director of operations, including decisions to hire, fire, advance, promote or change status.
* Responsible for overall quality of patient care and clinical performance of nurses and aides.
* Organizes clinical operations for the care center.
* Reviews requests for services and determines patient eligibility/suitability for home care services. Works with intake in coordinating patient referrals and admissions.
* Oversees scheduling.
* Oversees payor verification and precertification requirements.
* Reviews documentation of other staff members and ensures missing, incomplete and/or untimely documentation issues are resolved.
* Assists clinicians in establishing immediate and long-term patient goals, setting priorities and developing Plan of Care (POC).
* Regularly evaluates the needs of the patient and makes necessary revisions to the plan of care in collaboration with clinicians.
* May provide direct patient care on an infrequent basis in times of emergency.
* Participates in the on-call process.
* Assists with training of staff to ensure quality care, compliance and fiscal responsibility.
* Participates in the investigation and resolution of patient/family/physician concerns.
Qualifications
* Associate or bachelor's degree in nursing.
* Current RN license, specific to the state(s) you are assigned to work.
* One year of clinical RN experience in home health or hospice.
* One year of RN management experience.
* Current CPR certification.
Our compensation reflects the cost of labor across several U.S. geographic markets and may vary depending on location, job-related knowledge, skills, and experience.
Amedisys is an equal opportunity employer. All qualified employees and applicants will receive consideration for employment without regard to race, color, religion, sex, age, pregnancy, marital status, national origin, citizenship status, disability, military status, sexual orientation, genetic predisposition or carrier status or any other legally protected characteristic.
* Associate or bachelor's degree in nursing.
* Current RN license, specific to the state(s) you are assigned to work.
* One year of clinical RN experience in home health or hospice.
* One year of RN management experience.
* Current CPR certification.
Our compensation reflects the cost of labor across several U.S. geographic markets and may vary depending on location, job-related knowledge, skills, and experience.
Amedisys is an equal opportunity employer. All qualified employees and applicants will receive consideration for employment without regard to race, color, religion, sex, age, pregnancy, marital status, national origin, citizenship status, disability, military status, sexual orientation, genetic predisposition or carrier status or any other legally protected characteristic.
* Recommends employment decisions for staff to the director of operations, including decisions to hire, fire, advance, promote or change status.
* Responsible for overall quality of patient care and clinical performance of nurses and aides.
* Organizes clinical operations for the care center.
* Reviews requests for services and determines patient eligibility/suitability for home care services. Works with intake in coordinating patient referrals and admissions.
* Oversees scheduling.
* Oversees payor verification and precertification requirements.
* Reviews documentation of other staff members and ensures missing, incomplete and/or untimely documentation issues are resolved.
* Assists clinicians in establishing immediate and long-term patient goals, setting priorities and developing Plan of Care (POC).
* Regularly evaluates the needs of the patient and makes necessary revisions to the plan of care in collaboration with clinicians.
* May provide direct patient care on an infrequent basis in times of emergency.
* Participates in the on-call process.
* Assists with training of staff to ensure quality care, compliance and fiscal responsibility.
* Participates in the investigation and resolution of patient/family/physician concerns.
$80k-95k yearly 60d+ ago
Clinical Response Coordinator - Legacy of Hope
University of Alabama at Birmingham 3.7
Clinical coordinator job in Montgomery, AL
Schedule: Shift May Vary Benefits include: 100% tuition assistance, wellness initiatives, generous paid time off, paid parental leave, Public Service Loan Forgiveness Program eligible employer, plus more. In addition to our many benefits and perks, UAB Medicine provides a variety of resources to support employees both personally and professionally.
The Clinical Response Coordinator (CRC) is an integral role within the organ donation process at Legacy of Hope (LoH). The CRC will be responsible for performing on-site visits to donor hospitals within their coverage area. They, in conjunction with the administrator on call, will determine initial suitability of potential organ and tissue donors. This will be done by communicating and interacting with hospital and physician staff in collaborative and professional ways. The CRC will evaluate specific case dynamics and determine which information is clinically significant and should be communicated to the hospital teams and Legacy of Hope staff who are off-site. They will also assess available clinical data found in medical record or bedside assessment to determine initial medical suitability for donation. The CRC will encourage implementation of catastrophic brain injury guidelines as appropriate based upon their clinical judgement. In situations when needed, the CRC will also be expected to identify and support the needs of the potential donor family and offer them information about donation opportunities (organ and tissue). After authorization is obtained, the CRC will coordinate the transport of blood for serological testing and tissue typing to the appropriate laboratories. They will also initiate individualized case donor management, after brain death is declared, to ensure donor stability while coordinating arrival of procurement transplant coordinator (PTC) or critical care transport (CCT) to donor's location. Donor management could include ordering and interpreting labs, ensuring appropriate fluid maintenance, and implementing vasoactive and hemodynamic supportive medications as required by the donor's status. They will obtain required information from the hospital medical record to be transferred with patients from the donor hospital location to the donor recovery center as appropriate.
The Clinical Response Coordinator will also be able to perform specific partner services activities as directed by their supervisor. Those responsibilities may include but not be limited to: rounding through units to build relationships, presenting information/outcomes to hospital staff members in both formal and informal settings, and participating in education about donor suitability, brain death testing, specific donation processes, etc. This position requires 12-15 days of 24-hour call per month.
Position Requirements:
EDUCATION AND EXPERIENCE:
Required: Associate's degree in a medical or related field and one (1) year of experience in nursing, as an EMT, Paramedic, Respiratory Therapist, Social Worker, or experience in the donation industry required. Work experience may substitute for education requirement.
Preferred: Hospital experience, crisis intervention, and/or grief support.
.
LICENSE, CERTIFICATION AND/OR REGISTRATION:
Required: Valid driver's license and ability to be insured.
Preferred: Currently licensed/certified as a Nurse, Emergency Medical Technician (EMT), Paramedic, Respiratory Therapist, Social Worker, or related.
TRAITS & SKILLS: Must be self-directed / self-motivated; must have good communication and interpersonal skills. Must be able to: (1) perform a variety of duties often changing from one task to another of a different nature without loss of efficiency or composure; (2) accept responsibility for the direction, control and planning of an one's own work; (3) work independently and on a flexible schedule; (4) recognize the rights and responsibilities of patient confidentiality; (5) convey empathy and compassion to those experiencing pain, physical or emotional distress and/or grief; (6) relate to others in a manner which creates a sense of teamwork and cooperation; (7) communicate effectively with people from every socioeconomic, cultural and educational background; (8) exhibit flexibility and cope effectively in an ever-changing, fast-paced healthcare environment; (9) perform effectively when confronted with emergency, critical, unusual or dangerous situations; (10) demonstrate the quality work ethic of doing the right thing the right way; and (11) maintain a customer focus and strive to satisfy the customer's perceived needs.
UA Health Services Foundation (UAHSF) is proud to be an AA/EOE/M/F/Vet/Disabled employer.
$35k-45k yearly est. 60d+ ago
Clinical Supervisor
Youth Villages 3.8
Clinical coordinator job in Auburn, AL
For over 35 years, Youth Villages has transformed the lives of children and families nationwide through innovative, research-based programs focused on preserving and restoring families.
As a national leader in children's mental and behavioral health, we serve more than 47,000 youth, young people, and their families annually across 29 states and Washington, D.C. Our proven treatment models drive long-term success in child welfare, juvenile justice, and mental health systems. At Youth Villages, we do what works - partnering with others to expand our impact and advocate for meaningful, lasting change.
We're seeking purpose-driven individuals who are passionate about making a difference. With a dedicated team of more than 5,000 staff, Youth Villages is committed to investing in and supporting our employees by offering opportunities to build a fulfilling career through professional growth, personal development, and a mission that matters- helping children and families live successfully.
For more information, please visit *********************
Program Overview:
Intercept , developed by Youth Villages, is an evidence-based intensive, in-home program that focuses on keeping families together by preventing out-of-home placements or facilitating reunification after such placements, including foster care, residential treatment facilities, hospitalization, or juvenile detention centers. It is one of the first programs to receive the well-supported designation from Title IV-E Prevention Services Clearinghouse developed in accordance with the Family First Prevention Services Act (FFPSA) having been shown to reduce out-of-home placements and accelerate permanency for children.
This program serves youth from birth to age 18 who are facing serious emotional or behavioral challenges or have experienced trauma, such as abuse or neglect. Services are provided by highly trained Family Intervention Specialists directly in the family's home and community-Intercept is not an office-based program.
Intercept provides intensive, strength-based support tailored to each family's unique needs, ultimately helping them achieve lasting change through evidence-based mental health interventions, along with the development of new parenting and communication skills.
Essential Duties and Responsibilities:
The Clinical Supervisor:
Provides on-call crisis support and intervention 24/7 (schedules vary by location)
Provides clinical direction to counselors and specialists during group supervision meetings held weekly
Oversees treatment planning, case management, and case progress
Participates in program meetings with other Clinical Supervisors as well as personal development meetings with Regional Supervisor and/or Licensed Program Expert
Provides and/or coordinates staff development
Reviews and approves clinical and organizational documentation (including but not limited to: timecards, mileage, and cell phone reimbursements) completed by their direct reports
Assists in the hiring and training process of new staff as needed
Provides support and coverage to help counselors and specialists manage their duties and responsibilities
Assists in the marketing/referral process to increase and strengthen program growth
Completes accurate and timely documentation in an electronic medical record system (EMR)
Performs other duties as assigned
Additional Information:
Schedule is flexible and non-traditional as it is based around the availability of youth and families served.
Applicants must possess a current, valid driver's license, an automobile for work purposes, and proof of auto insurance.
Community-based staff will be reimbursed for applicable mileage.
Qualifications:
Master's degree in a social services discipline (preferred)
Bachelor's degree in a social services discipline (required)
Degrees that can be considered include: social work, drug and alcohol education or counseling, psychology, criminal justice, guidance counseling, or marriage and family therapy (others subject to review)
Previous supervisory experience (preferred)
At least 6 months experience working with the intensive in-home services (strongly preferred)
Strong organizational skills and attention to detail
Excellent written, verbal, and oral skills
Ability to manage multiple priorities simultaneously
Basic computer knowledge
Ability to maintain a flexible schedule
Youth Villages Benefits
Medical, Dental, Prescription Drug Coverage and Vision
401(k)
Time off:
2 week paid vacation (full-time) / 1 week paid vacation (part-time)
12 paid sick days per year
11 paid holidays
Paid Parental Leave
Mileage & Cell Phone Reimbursement (when applicable)
Tuition reimbursement and licensure supervision
Growth & development through continuous training
Clinical and administrative advancement opportunities
*Benefits are excluded for variable status employees.
Youth Villages is an equal opportunity employer and provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
Youth Villages is committed to not only advancing diversity, equity, and inclusion in the workplace but also in our work with children and young adults. We know that children, families and young people of color can face inequity in child welfare and justice systems, and we train our employees to build the skills they need to work with the communities that we serve, as well as, other employees from different cultures and backgrounds. Youth Villages is opposed to racism in any of its forms and is committed to inclusion, equity, and diversity. We believe that respect for each other is crucial in the work that we do each day.
$41k-57k yearly est. Auto-Apply 5d ago
Clinical Response Coordinator - Legacy of Hope
Uahsf
Clinical coordinator job in Montgomery, AL
Schedule: Shift May Vary Benefits include: 100% tuition assistance, wellness initiatives, generous paid time off, paid parental leave, Public Service Loan Forgiveness Program eligible employer, plus more. In addition to our many benefits and perks, UAB Medicine provides a variety of resources to support employees both personally and professionally.
The Clinical Response Coordinator (CRC) is an integral role within the organ donation process at Legacy of Hope (LoH). The CRC will be responsible for performing on-site visits to donor hospitals within their coverage area. They, in conjunction with the administrator on call, will determine initial suitability of potential organ and tissue donors. This will be done by communicating and interacting with hospital and physician staff in collaborative and professional ways. The CRC will evaluate specific case dynamics and determine which information is clinically significant and should be communicated to the hospital teams and Legacy of Hope staff who are off-site. They will also assess available clinical data found in medical record or bedside assessment to determine initial medical suitability for donation. The CRC will encourage implementation of catastrophic brain injury guidelines as appropriate based upon their clinical judgement. In situations when needed, the CRC will also be expected to identify and support the needs of the potential donor family and offer them information about donation opportunities (organ and tissue). After authorization is obtained, the CRC will coordinate the transport of blood for serological testing and tissue typing to the appropriate laboratories. They will also initiate individualized case donor management, after brain death is declared, to ensure donor stability while coordinating arrival of procurement transplant coordinator (PTC) or critical care transport (CCT) to donor's location. Donor management could include ordering and interpreting labs, ensuring appropriate fluid maintenance, and implementing vasoactive and hemodynamic supportive medications as required by the donor's status. They will obtain required information from the hospital medical record to be transferred with patients from the donor hospital location to the donor recovery center as appropriate.
The Clinical Response Coordinator will also be able to perform specific partner services activities as directed by their supervisor. Those responsibilities may include but not be limited to: rounding through units to build relationships, presenting information/outcomes to hospital staff members in both formal and informal settings, and participating in education about donor suitability, brain death testing, specific donation processes, etc. This position requires 12-15 days of 24-hour call per month.
Position Requirements:
EDUCATION AND EXPERIENCE:
Required: Associate's degree in a medical or related field and one (1) year of experience in nursing, as an EMT, Paramedic, Respiratory Therapist, Social Worker, or experience in the donation industry required. Work experience may substitute for education requirement.
Preferred: Hospital experience, crisis intervention, and/or grief support.
.
LICENSE, CERTIFICATION AND/OR REGISTRATION:
Required: Valid driver's license and ability to be insured.
Preferred: Currently licensed/certified as a Nurse, Emergency Medical Technician (EMT), Paramedic, Respiratory Therapist, Social Worker, or related.
TRAITS & SKILLS: Must be self-directed / self-motivated; must have good communication and interpersonal skills. Must be able to: (1) perform a variety of duties often changing from one task to another of a different nature without loss of efficiency or composure; (2) accept responsibility for the direction, control and planning of an one's own work; (3) work independently and on a flexible schedule; (4) recognize the rights and responsibilities of patient confidentiality; (5) convey empathy and compassion to those experiencing pain, physical or emotional distress and/or grief; (6) relate to others in a manner which creates a sense of teamwork and cooperation; (7) communicate effectively with people from every socioeconomic, cultural and educational background; (8) exhibit flexibility and cope effectively in an ever-changing, fast-paced healthcare environment; (9) perform effectively when confronted with emergency, critical, unusual or dangerous situations; (10) demonstrate the quality work ethic of doing the right thing the right way; and (11) maintain a customer focus and strive to satisfy the customer's perceived needs.
UA Health Services Foundation (UAHSF) is proud to be an AA/EOE/M/F/Vet/Disabled employer.
$40k-56k yearly est. 60d+ ago
Hospice Clinical Manager for Christian provider
Empyrean Hospice 4.0
Clinical coordinator job in Columbus, GA
We are a Christian hospice offering the highest quality clinical care and the love and salvation of Jesus Christ.
Empyrean Hospice hires Clinical Managers for the overall direction of hospice branch's clinical services. The Clinical Manager establishes, implements, and evaluates goals and objectives that meet and promote our standards of quality and compassionate care delivery.
Salary or hourly rate listed is the base for this role; increase commensurate with experience.
Position Overview - Clinical Manager:
• Represents Empyrean Hospice with the utmost professionalism and compassion
• Assists in the development of organization goals
• Develops, recommends, and administers policies and procedures
• Manages the daily operations of the branch, its staff, the patients in its care or considering its care, and community relationships regarding hospice education and services
• Coordinates and oversees all direct and indirect patient services and assures the quality and safe delivery of hospice services
• Provides guidance and counseling to the team for continual improvement in all aspects of care
• Promotes hospice referrals in the health care community.
• Assists with budget preparation and administration
• Interprets operational indicators that could impact staffing levels, revenue, or expenses
• Hires and orients personnel and conducts performance evaluations
• Assures proper maintenance of clinical records in compliance with local, state, and federal laws
• Maintains appropriate inventory of supplies and equipment for the provision of patient care
• Plans and implements in-service and continuing education programs
• Assures compliance with all local, state, and federal laws regarding licensure and certification of organization personnel and, maintains compliance to the CHAP Home Care standards
• Stays informed and shares knowledge of changes in the field of nursing and hospice care
• In the absence of the Executive Director/Administrator, the Clinical Manager will be vested with authority to act on their behalf
• Ensures standards of ethical business and clinical practice are prioritized
Who is Empyrean Hospice?
With Empyrean Hospice, we are family. We are committed to caring for people at end of life with the same level of dedication and compassion we would choose for our own loved ones. Our core values are the foundation for our dedication to integrity and clinical excellence.
Empyrean is a national company with community heart. We provide resources and leadership to support our care teams across the country so they can focus on the quality-of-life care and clinical excellence for the patients and families we serve. Our culture fosters a focus on our care delivery with work-life balance and support for our team members through manageable caseloads and professional growth supported by a team of expert leaders.
Empyrean offers ongoing professional education opportunities, manageable caseloads, and a benefits package for eligible employees.
• Competitive compensation
• Comprehensive benefits include paid time off (PTO), dental, health, life, and vision insurance, an employee assistance program, and professional development assistance
• Mileage reimbursement plan
• Opportunities for professional growth and advancement
Position Qualifications
• Professionalism, compassion, empathy, and a desire to help others
• Initiative-taking, organized, with attention to detail
• Registered nurse in the state with current licensure to practice professional nursing in the state
• Bachelor's degree in nursing from an accredited program by the National League for Nursing and/or master's degree in hospice preferred
• One (1) to two (2) years of recent experience in home care
• One (1) year of management experience preferred with demonstrated ability to supervise and direct personnel
• Interpersonal skills and ability to deal tactfully with the community
• Has excellent observation, verbal, and written communication skills
• Knowledge of business management, governmental regulations, and CHAP standards
• Must be flexible in work hours
• Must possess a willingness to maintain comprehensive working knowledge regarding information systems and applicable software programs; Computer proficient with Microsoft suite; preferred experience with Homecare Homebase or other EMR
• Understands hospice care and the services provided to patient and family/caregiver
• Intimate knowledge of Medicare Hospice Certification
Empyrean Hospice is an equal opportunity employer and considers all qualified applicants equally without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or veteran status.
Candidates for employment with Empyrean understand that Empyrean expressly does not want employees to use, and employee's responsibilities and duties with Empyrean will not require or involve, any trade secrets or other confidential information secrets that employee may have obtained from former employers or any other third party. Further, Empyrean expects and facilitates disclosure of, and compliance with, any obligations with any prior employers or other third parties that may legally apply to an employee.
$53k-88k yearly est. Auto-Apply 60d+ ago
Clinic Manager - Columbus/Macon
Georgia Spine & Orthopedics
Clinical coordinator job in Columbus, GA
Job DescriptionDescription:
Georgia Spine & Orthopaedics is a leading healthcare facility that provides exceptional orthopedic and spine care to our community. Committed to excellence in patient outcomes, innovative medical practices, and a patient-centered approach, we are seeking an experienced Clinic Manager to contribute to the success of our organization.
We are seeking a proactive and organized Clinic Manager to oversee both administrative and clinical operations in Columbus and Macon. The successful candidate will play a vital role in maintaining efficient office processes, promoting a positive work environment, and supporting the overall success of our team.
Clinic Manager Responsibilities
Manage day-to-day administrative and clinical operations, including scheduling, patient flow, appointment coordination, and inquiries.
Supervise and support administrative staff, providing guidance and fostering a collaborative and positive work environment.
Implement and enforce office policies and procedures to ensure smooth operations and compliance with healthcare regulations.
Coordinate and collaborate with various departments to optimize workflow and communication.
Manage inventory, order supplies, and maintain relationships with vendors.
Develop and maintain effective filing systems and electronic records to ensure data integrity.
Handle patient concerns and inquiries, ensuring a high level of customer service.
Support the recruitment, training, and development of administrative staff.
Collaborate with leadership to implement improvements in office efficiency and patient experience
Requirements:
• Proven experience as an Office Manager, preferably in a healthcare setting.
• Medical Assistant Experience Required
• Strong organizational and multitasking skills.
• Excellent communication and interpersonal abilities.
• Familiarity with healthcare regulations and compliance.
• Proficient in office software (e.g., Microsoft Office, electronic health records systems).
• Ability to work collaboratively with a diverse team.
• Detail-oriented and committed to maintaining confidentiality.
Clinic Manager Benefits and Perks
• Excellent benefits package including medical, dental, vision, and multiple add-ons available.
• Paid time off
• Paid holidays
• Mileage reimbursement and travel stipends are available.
$48k-82k yearly est. 9d ago
Intake Coordinator Supervisor The Bradley Center, Full Time Day
Scionhealth
Clinical coordinator job in Columbus, GA
At ScionHealth, we empower our caregivers to do what they do best. We value every voice by caring deeply for every patient and each other. We show courage by running toward the challenge and we lean into new ideas by embracing curiosity and question asking. Together, we create our culture by living our values in our day-to-day interactions with our patients and teammates.
Job Summary
Lead the Admissions/Intake Services department at The Bradley Center through providing administrative and clinical leadership to the department. Analyze, monitor, and lead the daily operations of the admissions department through evaluating, recommending, and implementing workflow in order to maintain optimal standards of patient care. Responsible for evaluating performance against established expectations and standards.
Leadership Capabilities
Provide leadership, direction and growth opportunities to members of the department, performing those responsibilities in accordance with the Hospital's policies and applicable laws. Responsible for participating in interviewing, hiring, planning, assigning or directing work, appraising performance, disciplining team members and resolving problems.
Essential Functions
* Provides clinical and administrative leadership and supervision of the Patient Access department.
* Establishes and communicates expectations and standards to associates; monitors performance and provides effective feedback and coaching.
* Coordinates resources to obtain recommended treatment.
* Develops, cultivates, and maintains internal and external relationships within the community and region.
* Educates the community and promote the services of The Bradley Center; provides appropriate resources to the community.
* Oversees the proper utilization of financial and human resource assets.
* Collaborates with Utilization Review to monitor and provide for the appropriate utilization of hospital-based services to meet payer guidelines.
Qualifications
Education
* Master's degree in Nursing, Psychology, Sociology, or related field Required
Required Skills
* Requires critical thinking skills, decisive judgment and the ability to work with minimal supervision.
* Must be able to work in a stressful environment and take appropriate action.
Licenses/Certifications
* Licensed Clinical Social Worker (LCSW, Licensed Professional Counselor (LPC), or Licensed MSN.
* Licensed Clinical Social Worker (LCSW) or Licensed Professional Counsel (LPC).
* Valid Driver's License.
Experience
* Three (3) years of behavior health experience.
$30k-41k yearly est. 41d ago
Intake Coordinator-RN
Universal Health Services 4.4
Clinical coordinator job in Montgomery, AL
Responsibilities Intake Coordinator- RN- PRN Horizon Health is seeking a Clinical Assessment Coordinator for our unit at Baptist Health in Montgomery, AL. The Clinical Assessment Coordinator, in conjunction with the unit's Program Director may coordinate the referral development and pre-admission patient assessment process and provide clinical assessments for potential clients.
Responsibilities:
* In coordination with the Program Director, develops, implements, coordinates, and evaluates clinical admission, referrals, and/or discharge processes.
* Conducts on and off site patient assessments, including appropriate test administration, interpretation and recommendations
* Responds to intake calls and completes admission paperwork
* Participates in the development of treatment plans in coordination with the treatment team
* Coordinates treatment with physicians and other health and social agencies
* Facilitates groups, family and individual sessions and completes all necessary documentation
* Coordinates and participates as a direct liaison with appropriate interested parties and physicians through the patient referral inquiry, admission, treatment, and discharge process
* Reviews newly admitted patient accounts for eligibility and authorization daily
* Maintains schedule for filing court paperwork and hearings
* Addresses issues in a timely manner including crisis and higher level of care referrals.
* Other Duties as Assigned
Benefit Highlights:
* Competitive Compensation
* Excellent Medical, Dental, Vision, and Prescription Drug Plan
* 401(K) with company match and discounted stock plan
* Long and Short-term Disability
* Flexible Spending Accounts; Healthcare Savings Account
* Life Insurance
* Career development opportunities within the company
* Tuition Assistance
* Rewarding work environment - Enjoy going to work every day!
Who we are & where you can make a difference:
Quality care is our passion; improving lives is our reward. Horizon Health, a subsidiary of Universal Health Services, is a leading behavioral services management company. Horizon Health Behavioral Health Services has been leading the way in partnering with hospitals to manage their behavioral health programs for over 40 years. With an unparalleled breadth of services, Horizon Health has singular expertise in behavioral health conditions and comprehensive care settings. Whether it involves the planning, development and implementation of a new behavioral health service line, or the successful management of an existing behavioral health service, Horizon Health has extensive expertise in successfully addressing concerns unique to hospital-based programs.
About Universal Health Services:
One of the nation's largest and most respected providers of hospital and healthcare services, Universal Health Services, Inc. (NYSE: UHS) has built an impressive record of achievement and performance, growing since its inception into a Fortune 500 corporation. Headquartered in King of Prussia, PA, UHS has 99,000 employees. Through its subsidiaries, UHS operates 28 acute care hospitals, 331 behavioral health facilities, 60 outpatient and other facilities in 39 U.S. States, Washington, D.C., Puerto Rico and the United Kingdom.
For more information about the position, contact Courtney Eble, Healthcare recruiter, at *******************************
Qualifications
* Bachelor's degree in Nursing
* Active AL or multi-state RN license
* 3 years of experience in healthcare required
* Behavioral health experience required
EEO Statement
All UHS subsidiaries are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants and teammates. UHS subsidiaries are equal opportunity employers and as such, openly support and fully commit to recruitment, selection, placement, promotion and compensation of individuals without regard to race, color, religion, age, sex (including pregnancy, gender identity, and sexual orientation), genetic information, national origin, disability status, protected veteran status or any other characteristic protected by federal, state or local laws.
We believe that diversity and inclusion among our teammates is critical to our success.
Avoid and Report Recruitment Scams
At UHS and all our subsidiaries, our Human Resources departments and recruiters are here to help prospective candidates by matching skillset and experience with the best possible career path at UHS and our subsidiaries. During the recruitment process, no recruiter or employee will request financial or personal information (e.g., Social Security Number, credit card or bank information, etc.) from you via email. Our recruiters will not email you from a public webmail client like Hotmail, Gmail, Yahoo Mail, etc.
If you suspect a fraudulent job posting or job-related email mentioning UHS or its subsidiaries, we encourage you to report such concerns to appropriate law enforcement. We encourage you to refer to legitimate UHS and UHS subsidiary career websites to verify job opportunities and not rely on unsolicited calls from recruiters.
$24k-30k yearly est. Easy Apply 6d ago
Per Diem / PRN Nurse RN - Clinical Nurse Coordinator - $44-48 per hour
Pyramid Consulting 4.1
Clinical coordinator job in LaGrange, GA
Per Diem / PRN Nurse RN - Clinical Nurse Coordinator - $44-48 per hour at Pyramid Consulting summary: This role is for a Per Diem / PRN Registered Nurse Clinical Nurse Coordinator providing patient-centered care across multiple hospital units in LaGrange, Georgia. The position involves assessment, care planning, collaboration with interdisciplinary teams, patient teaching, and promoting evidence-based practices. Candidates must hold an active RN license, have acute care experience, and demonstrate strong communication and critical-thinking skills.
Pyramid Consulting is seeking a per diem / prn nurse RN Clinical Nurse Coordinator for a per diem / prn nursing job in LaGrange, Georgia.
Job Description & Requirements
• Specialty: Clinical Nurse Coordinator
• Discipline: RN
• Start Date:
• Duration: Ongoing
• Shift: 12 hours, days
• Employment Type: Per Diem
? Registered Clinical Nurse (RN) - PRN Float | Day Shift | LaGrange, GA ?
? Pay: $44/hr - $48/hr (open for negotiation)
? Location: LaGrange, Georgia
? Schedule: PRN | Day Shift
About the Role
Join a dynamic, patient-focused healthcare team where your expertise truly matters! As a Registered Clinical Nurse (RN) - PRN Float, you'll be part of an interdisciplinary care team dedicated to providing exceptional patient-centered care across multiple units. This flexible float position allows you to make a meaningful impact in various departments while building diverse clinical experience in a supportive, collaborative environment.
You'll play a vital role in assessment, care planning, implementation, and evaluation - ensuring each patient receives the highest quality of care guided by evidence-based practices and compassionate service.
✨ What You'll Do
✅ Deliver exceptional, individualized patient care across diverse units.
✅ Collaborate with interdisciplinary teams to achieve the best clinical outcomes.
✅ Participate in patient teaching, bedside shift reporting, and care coordination.
✅ Support and mentor other nurses, fostering a positive and growth-oriented environment.
✅ Promote evidence-based practices and continuous improvement initiatives.
✅ Practice within established ethical, clinical, and professional nursing standards.
? What We're Looking For
• Education: Associate's Degree in Nursing required; BSN preferred.
• Experience: Minimum 1 year of recent acute care clinical experience required.
• License/Certifications:
- Active RN license (GA or Multi-State Compact).
- BLS required; ACLS preferred.
- National certification in specialty area preferred.
• Skills: Excellent communication, teamwork, and critical-thinking abilities.
? Why Join Us
Be part of an organization that values compassion, excellence, and collaboration. Here, your ideas matter - your voice helps shape how care is delivered, and your commitment to patients inspires everyone around you.
Comprehensive Benefits Package:
? Health, Dental, and Vision Insurance
? 403(b) Retirement Plan with Employer Match
? Paid Time Off (PTO) and Holiday Pay
? Sign-On Bonus and Relocation Assistance (for eligible roles)
Why You'll Love Working Here:
? Modern, well-equipped campus with a positive, team-driven culture.
?️ Located in a beautiful area surrounded by lakes, parks, and scenic trails - perfect for work-life balance.
? Supportive leadership, continuous education opportunities, and pathways for career advancement.
? Inclusive environment that celebrates diversity and encourages personal growth.
Ready to Take the Next Step?
Join a team where your nursing expertise makes a real difference - every shift, every patient, every day.
Apply now and take the opportunity to build a career that's as inspiring as it is rewarding.
About Pyramid Consulting
Supercharge your career with Pyramid Consulting.
We are dedicated to accelerating growth, creating opportunities, and fostering an environment built on belonging, trust, and mutual respect. Our commitment is to help you find the best path to achieve your career goals.
As a global leader in workforce and technology solutions, Pyramid Consulting, Inc. partners with clients to navigate competitive and ever-changing markets. Our award-winning family of brands - Pyramid Talent, Celsior, and GenSpark - works seamlessly together, delivering integrated solutions through multiple delivery models across five continents and 25+ countries. Since our founding in 1996, we've supported 125+ Fortune 500 companies across all major industries by engaging 6,500+ consultants worldwide.
Join our talent network
Looking for a job that aligns with your skills and ambitions? Join our talent network and enhance your job search experience with access to a broad range of job opportunities tailored to your background and interests.
• Explore jobs: Visit our job portal to browse positions that suit your preferences. You can filter jobs by role, location, or industry to find the best match.
• Apply: Submit your application and upload your resume through our portal. Our recruiters will reach out to discuss your career goals and help connect you with the right opportunities.
Take the next step in your career journey with Pyramid Consulting, where we're committed to helping you grow and succeed.
Keywords:
Registered Nurse, Clinical Nurse Coordinator, Per Diem Nurse, PRN Nurse, Acute Care, Patient Care, Evidence-Based Practice, Care Coordination, Healthcare Nursing, Interdisciplinary Team
Teach courses and implement the instructional program in accordance with course syllabi, Alabama Community College System policies and guidelines; advise and recruit students; assist in updating curricula; maintain teaching equipment; coordinateclinicals; serve on College committees; support the total mission of the College; coordinate instructional activities with the Director of Nursing, and Dean where applicable; and perform other duties as assigned. Position requires extensive knowledge of the instructional discipline.
Salary Schedule-D1
Essential Duties and Responsibilities
* Perform assignments and maintain duty hours in accordance with the current faculty schedule. Classes may be taught at either campus and/or at an off-campus site. Classes may be scheduled day, evening or weekends to meet student needs.
* Teach courses as assigned in accordance with the course syllabi, facilitate student learning, and assist in implementing the total instructional program.
* Coordinateclinical schedules and sites for nursing students.
* Promote nursing student education and remediation methods.
* Provide instruction in nursing simulation/lab activities to include simulation development/objectives, pre-briefings, debriefings, and diverse scenarios.
* Integrate course specific simulation activities/scenarios to promote clinical judgement, critical thinking, and clinical reasoning.
* Run, assess, and maintain simulation activity records.
* Promote safety throughout the total instructional program.
* Maintain instructional related records including student attendance, student grades, enrollment records, competency records, student's plan of study, etc.
* Provide timely and accurate "Student No-Show" reports. These reports require instructor signatures and instructors are potentially financially liable for inaccurate reporting.
* Maintain classroom and laboratory equipment, supplies, and environments, which promote learning to perform in the current and emerging work world environments.
* Complete required surveys and student data requests.
* Communicate with program advisory committee members, employers, and former students to receive guidance for upgrading curriculum and instruction.
* Provide academic advisement and assistance to students in career decision-making program planning, registration, and job seeking.
* Follow-up on graduates and former students.
* Coordinate with the college placement office to identify potential employment opportunities for students and to identify students interested in job placement.
* Assist in developing and upgrading course syllabi and other curriculum materials.
* Manage live work activities, records, and materials where included in the curriculum.
* Serve on college committees as needed to support the total mission of the college.
* Promote the specific instructional program and the total institution within the occupational area and throughout the community.
* Recruit students for classes.
* Assist in recruiting, orienting, and supporting adjunct instructors to teach courses in area of responsibility.
* Contribute to the welfare and advancement of the total community.
* Keep up-to-date with teaching methodology, occupational information, and technology through professional development activities.
* Incorporate technology into the teaching/learning experience.
* Comply with applicable laws and regulations communicated through memos, staff meetings, and professional development workshops.
* Adhere to annual faculty evaluations.
* Develop and implement lesson plans, and appropriate test and measurement devices.
* Attend faculty meetings, in-service programs, and other college programs and functions, such as commencement and award ceremonies.
* Coordinateclinical activities and preceptorships with affiliate clinical agencies.
* Maintain expertise in areas of responsibility, and performance must reflect scholarship and evidenced based teaching and clinical practices.
* Participate fully in the institutional planning process and assist in carrying out the overall instructional mission of the College.
* Maintain compliance with College and program related accreditation and certification standards.
* Retain and submit documentation as requested to support accreditation efforts.
* Performs other duties as assigned by Director of Nursing and/or Dean.
Qualifications
Required Minimum Qualifications:
* Master's Degree or higher in Nursing from an accredited college or university.
* Minimum of 3 years full-time experience in Nursing.
* Ability to facilitate simulation learning for program requirements.
* Knowledge in statistical processes associated with exam item development, validity, and analysis.
* Ability to perform all clinical and lab duties.
* Ability to establish and maintain effective working relationships with students, other employees, and the public.
* The ability to project a professional and congenial demeanor.
* The ability to workday and evening hours dictated by the Nursing instructional schedule.
* Performance demonstrates effectiveness in assigned area(s) of responsibility.
Required License, Certifications, or Special Credentials:
* Basic Life Support (BLS) certification
* Current unencumbered Alabama Nursing License
Required Knowledge, Skills, & Abilities:
* Ability to facilitate simulation learning for program requirements.
* Ability to perform all clinical and lab duties.
* Ability to establish and maintain effective working relationships with students, other employees, and the public.
* Ability to project a professional and congenial demeanor.
* Ability to work day and evening hours dictated by the Nursing instructional schedule.
* Knowledge and experience with curriculum and new program development.
* Excellent oral and written communication skills.
* Ability to multi-task.
* Ability to plan, organize, coordinate, and manage complicated tasks.
* Ability to use email and Microsoft Word proficiently.
Application Procedures/Additional Information
Applicants must meet the minimum qualifications as indicated on this vacancy notice and must submit a completed online application packet to be considered for this position. Applicants who fail to submit all required information will not be considered. Only applications received during the period of this announcement will be considered. A complete application packet consists of:
* Trenholm State Community College online employment application.
* A current resume, including three (3) references.
* Copy of transcripts that demonstrate the required educational qualifications must be included and must identify the applicant, institution, degree, and date conferred.
WORK EXPERIENCE VERIFICATION
Neither a resume nor an application is appropriate verification of work experience. It is not our policy to contact current and/or previous employers to obtain employment verification. "Work experience verification is required in writing from your current and/or previous employer(s) confirming the required level of experience as stated in the "Minimum Qualifications" section and other related experience. Verification should include dates of employment and position title(s). Proof of work experience verification may be delayed until an official offer of employment using the Work Experience Verification form, which is found on the Human Resources home page. All work experience verification must be completed within 15 days following the employment offer.
APPLICATION DEADLINE: Complete application files will be accepted by the Office of Human Resources on a continuous basis and remain active for one year for available positions. Incomplete application packets will eliminate the possibility of a position opportunity.
EEOC, E-VERIFY, BACKGROUND CHECK STATEMENTS: Trenholm State Community College is an equal opportunity employer. It is the official policy of the Alabama Community College System that no person shall, on the grounds of race, color, disability, gender, religion, creed, national origin, or age, be excluded from participation in, be denied the benefits of, or be subjected to discrimination under any program, activity, or employment. Trenholm State Community College will make reasonable accommodations for qualified disabled applicants or employees.
Trenholm State Community College reserves the right to withdraw this job announcement at any time prior to the awarding. More than one position in the same job classification may be filled by the applicants for this position should another vacancy occur during the search process.
Any offer of employment is contingent upon the completion of a satisfactory criminal background investigation. The applicant will be responsible for the cost of the criminal background investigation.
This employer participates in E-Verify.
Teach courses and implement the instructional program in accordance with course syllabi, Alabama Community College System policies and guidelines; advise and recruit students; assist in updating curricula; maintain teaching equipment; coordinateclinicals; serve on College committees; support the total mission of the College; coordinate instructional activities with the Director of Nursing, and Dean where applicable; and perform other duties as assigned. Position requires extensive knowledge of the instructional discipline.
Salary Schedule-D1
* Perform assignments and maintain duty hours in accordance with the current faculty schedule. Classes may be taught at either campus and/or at an off-campus site. Classes may be scheduled day, evening or weekends to meet student needs.
* Teach courses as assigned in accordance with the course syllabi, facilitate student learning, and assist in implementing the total instructional program.
* Coordinateclinical schedules and sites for nursing students.
* Promote nursing student education and remediation methods.
* Provide instruction in nursing simulation/lab activities to include simulation development/objectives, pre-briefings, debriefings, and diverse scenarios.
* Integrate course specific simulation activities/scenarios to promote clinical judgement, critical thinking, and clinical reasoning.
* Run, assess, and maintain simulation activity records.
* Promote safety throughout the total instructional program.
* Maintain instructional related records including student attendance, student grades, enrollment records, competency records, student's plan of study, etc.
* Provide timely and accurate "Student No-Show" reports. These reports require instructor signatures and instructors are potentially financially liable for inaccurate reporting.
* Maintain classroom and laboratory equipment, supplies, and environments, which promote learning to perform in the current and emerging work world environments.
* Complete required surveys and student data requests.
* Communicate with program advisory committee members, employers, and former students to receive guidance for upgrading curriculum and instruction.
* Provide academic advisement and assistance to students in career decision-making program planning, registration, and job seeking.
* Follow-up on graduates and former students.
* Coordinate with the college placement office to identify potential employment opportunities for students and to identify students interested in job placement.
* Assist in developing and upgrading course syllabi and other curriculum materials.
* Manage live work activities, records, and materials where included in the curriculum.
* Serve on college committees as needed to support the total mission of the college.
* Promote the specific instructional program and the total institution within the occupational area and throughout the community.
* Recruit students for classes.
* Assist in recruiting, orienting, and supporting adjunct instructors to teach courses in area of responsibility.
* Contribute to the welfare and advancement of the total community.
* Keep up-to-date with teaching methodology, occupational information, and technology through professional development activities.
* Incorporate technology into the teaching/learning experience.
* Comply with applicable laws and regulations communicated through memos, staff meetings, and professional development workshops.
* Adhere to annual faculty evaluations.
* Develop and implement lesson plans, and appropriate test and measurement devices.
* Attend faculty meetings, in-service programs, and other college programs and functions, such as commencement and award ceremonies.
* Coordinateclinical activities and preceptorships with affiliate clinical agencies.
* Maintain expertise in areas of responsibility, and performance must reflect scholarship and evidenced based teaching and clinical practices.
* Participate fully in the institutional planning process and assist in carrying out the overall instructional mission of the College.
* Maintain compliance with College and program related accreditation and certification standards.
* Retain and submit documentation as requested to support accreditation efforts.
* Performs other duties as assigned by Director of Nursing and/or Dean.
Required Minimum Qualifications:
* Master's Degree or higher in Nursing from an accredited college or university.
* Minimum of 3 years full-time experience in Nursing.
* Ability to facilitate simulation learning for program requirements.
* Knowledge in statistical processes associated with exam item development, validity, and analysis.
* Ability to perform all clinical and lab duties.
* Ability to establish and maintain effective working relationships with students, other employees, and the public.
* The ability to project a professional and congenial demeanor.
* The ability to workday and evening hours dictated by the Nursing instructional schedule.
* Performance demonstrates effectiveness in assigned area(s) of responsibility.
Required License, Certifications, or Special Credentials:
* Basic Life Support (BLS) certification
* Current unencumbered Alabama Nursing License
Required Knowledge, Skills, & Abilities:
* Ability to facilitate simulation learning for program requirements.
* Ability to perform all clinical and lab duties.
* Ability to establish and maintain effective working relationships with students, other employees, and the public.
* Ability to project a professional and congenial demeanor.
* Ability to work day and evening hours dictated by the Nursing instructional schedule.
* Knowledge and experience with curriculum and new program development.
* Excellent oral and written communication skills.
* Ability to multi-task.
* Ability to plan, organize, coordinate, and manage complicated tasks.
* Ability to use email and Microsoft Word proficiently.
Applicants must meet the minimum qualifications as indicated on this vacancy notice and must submit a completed online application packet to be considered for this position. Applicants who fail to submit all required information will not be considered. Only applications received during the period of this announcement will be considered. A complete application packet consists of:
* Trenholm State Community College online employment application.
* A current resume, including three (3) references.
* Copy of transcripts that demonstrate the required educational qualifications must be included and must identify the applicant, institution, degree, and date conferred.
WORK EXPERIENCE VERIFICATION
Neither a resume nor an application is appropriate verification of work experience. It is not our policy to contact current and/or previous employers to obtain employment verification. "Work experience verification is required in writing from your current and/or previous employer(s) confirming the required level of experience as stated in the "Minimum Qualifications" section and other related experience. Verification should include dates of employment and position title(s). Proof of work experience verification may be delayed until an official offer of employment using the Work Experience Verification form, which is found on the Human Resources home page. All work experience verification must be completed within 15 days following the employment offer.
APPLICATION DEADLINE: Complete application files will be accepted by the Office of Human Resources on a continuous basis and remain active for one year for available positions. Incomplete application packets will eliminate the possibility of a position opportunity.
EEOC, E-VERIFY, BACKGROUND CHECK STATEMENTS: Trenholm State Community College is an equal opportunity employer. It is the official policy of the Alabama Community College System that no person shall, on the grounds of race, color, disability, gender, religion, creed, national origin, or age, be excluded from participation in, be denied the benefits of, or be subjected to discrimination under any program, activity, or employment. Trenholm State Community College will make reasonable accommodations for qualified disabled applicants or employees.
Trenholm State Community College reserves the right to withdraw this job announcement at any time prior to the awarding. More than one position in the same job classification may be filled by the applicants for this position should another vacancy occur during the search process.
Any offer of employment is contingent upon the completion of a satisfactory criminal background investigation. The applicant will be responsible for the cost of the criminal background investigation.
This employer participates in E-Verify.
$56k-63k yearly est. 7d ago
REHABILITATION NURSE COORDINATOR
State of Alabama 3.9
Clinical coordinator job in Montgomery, AL
The Rehabilitation Nurse Coordinator is a permanent, full-time position with the Alabama Department of Rehabilitation Services. Positions are located throughout the state. This is advanced professional community health nursing work with Children's Rehabilitation Services.
$49k-57k yearly est. 60d+ ago
Medical - Nurse Coordinator
Sequel Youth Services 3.9
Clinical coordinator job in Montgomery, AL
Do you want to make a difference in the lives of our youth? Do you want a supportive work environment? A Little About Our Program ............. Established in 2013, Sequel Youth and Family Services at Montgomery is a licensed and academically accredited 20-bed residential treatment facility. The program specializes in treating adolescent females ages 12-18, with maladaptive sexual concerns and/or behavioral disorders. The campus is located in Montgomery, AL.
***************************
What is it like to work at a Sequel program! Check us out on Glassdoor or follow us on Facebook, or LinkedIn.
Position Overview:
Under the direction of the Clinical Director, the Nurse Coordinator will monitor resident status in order to ensure continuity of student care and to evaluate and/or initiate appropriateaction such as treatment and/or referral. Responsible for monitoring, reporting, charting and providing required reports for Improvement of Organizational Performance. Acts as infection Control Coordinator. Will work 12 hour shifts as approved by the administrator. This position requires experience in administering TB skin tests and blood draws. Qualifications:
This position requires a graduate from an approved LPN program. The candidatemust possess a valid unrestricted Practical Nursing License issued by the StateBoard of Nursing. Previous psychiatric and mental health nursing experiencewith an adolescent population is highly desirable. Must be able to deliverskilled nursing care in both routine and stressful periods.
The Perks:
Medical, Dental, Vision, and Life Insurance after 30 days Company provided Short-Term and Long-Term DisabilityCompany provided AD&D insurance Flexible Spending program 401K after sixty days Paid time off Employee Assistance ProgramsDaily PayDo you have what it takes?
Apply Now
How much does a clinical coordinator earn in Auburn, AL?
The average clinical coordinator in Auburn, AL earns between $34,000 and $66,000 annually. This compares to the national average clinical coordinator range of $43,000 to $77,000.