Clinical Research Coordinator Jobs in Glendale, CA

ESSENTIAL FUNCTION OF THE OPHTHALMIC TECHNICIAN/CLINICAL RESEARCH COORDINATOR: Responsible for the oversight, execution, and successful completion of study protocols Operates and upholds Good Clinical Practice (GCP) and Company Standard Operating Procedures (SOPs). Coordinates with all departments and team members to streamline operations and ensure the successful execution of patient study visits with quality and accurate data. RESPONSIBILITIES INCLUDE (but not limited to): Review and understand the protocol, Inclusion/Exclusion criteria, procedure manual, and eCRF guidelines for each clinical trial they are assigned to. Actively seeks to identify potential subjects from our database to prescreen and enroll in ongoing studies. Responsible for completing study specific assessments, and monitoring participants test results, including but not limited to Adverse Events, lab results, vitals, ECG, and other study procedures (escalating any protocol or safety concerns to the appropriate medical group and management.) Attends Site Initiation Visits, Investigator meetings (as requested), bi-weekly staff meetings, monitoring visits, and any other meetings that may arise. Responsible for overseeing all study subjects according to protocol specific requirements and GCP guidelines. Ensure lab and medical results are completed, and all eligibility requirements are met. Ensure quality assurance (QA) is performed on all electronic and paper source documents. Performs other related work as required and assigned by practice administrator or direct supervisor. REQUIREMENTS/ EXPERIENCE: Bilingual English and Spanish Minimum of 1 year of experience as an Ophthalmic Tehcnician Experience in: IOP, visual acuity, manifest refraction, fundus photography, OCT photography (preferred knowledge in Heidelberg), visual field, scribing, schirmers, corneal staining, pachymetry Preferred skills: Fluorescein Angiography, pupillometry Excellent interpersonal, verbal and written communication skills. Ability to effectively manage time with multiple and varied tasks with enthusiasm, prioritizing workload as needed. *PLEASE NOTE: We are based in Glendale, CA, and this is not a remote position.

If you are physically/mentally ill or healthy, get paid to trial new treatments and medications. This is a great way to earn additional income, sometimes from the comfort of your home. Participation in clinical trials can be a very rewarding experience. Not only do you get free access to cutting-edge medical treatment, but you are also contributing to science all whilst getting paid. Some of the conditions we are currently recruiting for include: Healthy participants Migraines Mental Health Issues Alzheimer's Disease Parkinson's Skin Conditions/Eczema Cancer COPD Diabetes Crohn's Children with Autism ..and many more Compensation can be up to several thousand dollars depending on the trial. No experience or education required.

Job Title : Clinical Research Informatician Job Duration : Direct Hire Salary : $125k - $140k *Must Have's:* - Bachelor's Degree in Health Information Management or Health Informatics OR B.S. in a clinical field (nursing, etc.) with certification in Health Informatics OR B.S. in informatics, computer science, statistics, biomedical engineering, artificial intelligence with certification in Health Informatics. *(Required)* - Master's Degree *(Preferred)* Minimum 2 years' experience in: Clinical Research Clinical Informatics Information Technology and/or Academic Healthcare Settings Experience with: Clinical operations, Health Information Management, or Care Management Clinical standards, coding, definitions, ontologies, dictionaries, and taxonomies Clinical Key Performance Indicators (KPIs) Implementing new technologies in clinical settings Healthcare data curation and documentation in a data warehouse Proficiency in: SQL and Python or similar coding languages Liaising between clinical stakeholders and technical teams Expertise in: Analyzing and optimizing clinical workflows to improve efficiency and patient outcomes Summary: The Clinical Research Informatician is a bridge between clinicians/researchers and data. They blend their knowledge of clinical workflow, terminology, and practices with an understanding of health information technology to advance clinical and translational research towards improved patient care. The Clinical Informatician will play an integral role focused on creating, testing, implementing, and maintaining applications and data for clinical areas. Responsibilities include acting as a liaison between clinicians/researchers and data stewards, interfacing with stakeholders on informatics software development, maintenance, and operations, and creating streamlined workflows for the exploitation of healthcare data. Minimum Education • Bachelor's Degree In Health Information Management or Health Informatics OR B.S. in clinical field (nursing, etc.) and certification in Health Informatics OR B.S. in informatics, computer science, statistics, biomedical engineering artificial intelligence AND certification in Health Informatics. Required • Master's Degree preferred Minimum Experience/Accountabilities • Minimum 2 years' experience in clinical research • Minimum 2 years' experience in clinical informatics • Minimum 2 years' experience in information technology and/or in academic healthcare setting • Experience with clinical operations, Health Information Management, or care management • Experience with clinical standards and coding • Experience with clinical definitions, ontologies, dictionaries, and taxonomies • Experience with KPIs as they relate to clinical areas • Experience implementing new technologies in clinical areas • Collect, organize, curate, and document healthcare information within the data warehouse. • Apply experience with clinical information and workflows to the development of informatics tools, applications, analyses, and procedures. • Develop, modify, test, and implement applications and algorithms for the collection, organization, and analysis of healthcare data. • Assist in the development of presentations, scientific publications, and grant proposals. • Apply insights gained from research to improve patient care or healthcare operations. • Ability to interact directly with and interpret healthcare data using self-service tools or coding languages, such as SQL and Python • Ability to liaison between clinical stakeholders and Enterprise Data & AI technical team members • Expertise in analyzing and optimizing clinical workflows, leveraging IT to enhance efficiency, accuracy, and patient outcomes through targeted interventions and system improvements. • Collaborate with software vendors and IT service providers to ensure that their products and services are tailored to meet the unique operational needs of the healthcare facility, optimizing performance and compliance.

This professional will report to Clinical Science and External Research (CSER) Leaders in the management of assigned clinical projects for the Cardiovascular Group to support the development of the evidence generation and dissemination strategy of assigned products, manage clinical studies, execute publication plans, and conduct literature reviews. S/he will manage activities with supervision consistent with level of experience. S/he will be responsible for providing support activities for clinical activities and other study-related tasks, as well as applicable department study-related procedures. The Senior Clinical Research Scientist will or may be responsible for: Working with Global Strategic Marketing, Franchise Clinical Leaders, Biostatistics, Data Management, Medical Affairs, and other functions on: (i) planning and executing research collaborations with physicians, (ii) tracking study idea development and progress, and (iii) planning data dissemination via congress presentation and peer-reviewed publications Managing nonregulated studies (eg, Investigator initiated, Registries, Real-world evidence, Company -sponsored postmarket studies) and low complexity regulated studies (eg, Postapproval, Real-world evidence) including study budget assessment, fair market value appraisal, contract development and execution, and payments Interfacing and collaborating with investigators, IRBs/ECs, Competent Authorities, contractors/vendors, and Company personnel Developing study-related materials (eg, protocol, CRFs, CSR) Analyzing, interpreting, summarizing, and sharing appropriate interpretation of clinical evidence generated from research studies Leading study-related publication efforts including abstracts, congress presentations, and manuscripts, per clinical publication policy Collaborating with cross-functional team members to develop collaterals to disseminate research results among internal and external stakeholders Knowing, understanding, incorporating, and complying with all applicable laws and regulations relating to business activities, and Policies and Procedures Evaluating publication support requests and providing meaningful, consolidated comments during the publication development lifecycle Tracking assigned project budgets to ensure adherence to business plans Communicating progress towards planned timelines Additional Skills Requirements: Effective time management, organizational and prioritization skills, and the ability to manage multiple tasks Strong project management skills with meticulous attention to detail and accuracy Professional verbal and written communication skills Proven ability to collaborate in a cross-functional team environment while having the skillset and confidence to work independently, as needed Must be reliable, and flexible in adapting to shifting business needs while contributing to a multidisciplinary and fast-paced working environment Must be a highly motivated, responsible, fast-learner, and team-oriented collaborator willing to take ownership of his/her contributions to the advancement of the collective CSER goals and objectives Proficient in Microsoft Office Qualifications: A minimum of a Bachelor's degree with at least 5 years of clinical research experience required Advance degree (Master's degree, PhD, PharmD etc.) with 2-3 year of clinical or related research experience highly preferred A Life Science, Physical Science, Nursing, or Biological Science degree is preferred Ability to analyze and interpret scientific data and advanced writing/presentation skills are required, such as conducting literature reviews, and planning and drafting conference presentation and peer-reviewed journal articles Knowledge of Good Clinical Practices and ICJME/Good Publication Practices is required Good understanding of clinical research science and processes along with an understanding of product development processes, team dynamics related to healthcare market environment, and global clinical trial regulations is preferred Prior experience designing and executing clinical studies is highly desirable Project management skills with the ability to handle multiple projects is required Medical device experience is preferred Cardiovascular experience is a plus Relevant industry certifications preferred (ie, CCRA, RAC, CDE, CMPP, MWC) This position is located in Irvine, CA

Role Description This is a full-time on-site role at a Clinical Research Center in Orange, CA. that specializes in GI diseases. We are seeking applicants for a Senior Clinical Research Coordinator with extensive clinical trial experience. The Senior CRC will work as a primary or secondary coordinator on Phase I/ II/III clinical trials in GI specialty. Qualifications Informed Consent and Protocol development skills Experience in Research, Clinical Research, and managing Clinical Trials Strong analytical and problem-solving abilities Excellent communication and interpersonal skills Detail-oriented and able to work effectively in a team Bachelor's degree in Human Resources, Psychology, Business, or a related field Job Duties Coordinate the day-to-day clinical operations of clinical research studies Perform study procedures in accordance with GCP and study protocols Organize and maintain paper and electronic study data in a complete and correct manner Work closely with recruitment and prescreening teams to meet study enrollment goals Conduct diagnostic, efficacy, and safety assessments as needed Mentor and lead less experienced coordinators and/or research assistants Take ownership of team productivity (enrollment) and quality metrics Job Requirements Five (5) or more years of industry-sponsored drug trial experience Demonstrated ability to work on high-enrolling Phase II/III clinical trials Attention to detail and the ability to handle multiple tasks with precision Demonstrated ability to work accurately and quickly with CTMS A command of professional spoken and written English Hours and Compensation This is a full-time employment position based in person at our clinic in Orange, CA. The starting salary for this position is $90,000 - $100,000 per year. A higher salary may be negotiable with candidates who have a valid nursing license (RN) and skills in infusions. The company pays for 75% of health, 99% of dental and vision, and 100% of life insurance for individual insurance costs for eligible full-time employees. Vacation (PTO) is earned at a rate of 3 weeks per year.

Gynecologic Oncology Clinical Research Coordinator Pay: $33.65 - $38.46 Schedule: Hybrid, Monday-Friday Responsibilities / Key Performance Indicators (KPIs): Patient Recruitment: Responsible for independently sourcing two patients per month. Patient Visits: Comfortable managing two patient visits per day, four days per week. Trial Support: Focus strictly on patient recruitment and visits; no regulatory or data management responsibilities required. Adaptability: Open to evolving processes and expectations within the role. Required Skills / Qualifications Gynecology Background: Experience in gynecology with flexibility to transition into oncology. Independence: Medium to high-functioning autonomy; ability to work with limited oversight while collaborating with experienced PIs. Flexibility: Willing to travel between sites and adapt to evolving requirements. Clinical Expertise: Proficient in conducting infusions and prioritizing patient care above all.

Hiring Organization: Rose International 476476 Job Title: Clinical Research Informatician Work Model: Hybrid Shift: candidates should ideally be available to come onsite one day a week, if needed. Employment Type: Permanent Min Hourly Rate($): 60.00 Max Hourly Rate($): 67.00 Must Have Skills/Attributes: Clinical, Healthcare, Management, Python, SQL Job Description ***Only qualified Clinical Research Informatician candidates located near the Los Angeles, CA area to be considered due to the position requiring an onsite presence*** Minimum Education: • Bachelor's Degree in Health Information Management or Health Informatics OR • B.S. in clinical field (nursing, etc.) and certification in Health Informatics OR • B.S. in informatics, computer science, statistics, biomedical engineering artificial intelligence AND certification in Health Informatics. • Master's Degree preferred Minimum Experience: • Minimum 2 years' experience in clinical research or clinical trials • Minimum 2 years' experience in clinical informatics • Minimum 2 years' experience in information technology and/or in academic healthcare setting • Experience with clinical operations, Health Information Management, or care management • Experience with clinical standards and coding • Experience with clinical definitions, ontologies, dictionaries, and taxonomies • Experience with KPIs as they relate to clinical areas • Experience implementing new technologies in clinical areas The Clinical Research Informatician is a bridge between clinicians/researchers and data. They blend their knowledge of clinical workflow, terminology, and practices with an understanding of health information technology to advance clinical and translational research towards improved patient care. The Clinical Informatician will play an integral role focused on creating, testing, implementing, and maintaining applications and data for clinical areas. Responsibilities include acting as a liaison between clinicians/researchers and data stewards, interfacing with stakeholders on informatics software development, maintenance, and operations, and creating streamlined workflows for the exploitation of healthcare data. Clinical Research Informatician Accountabilities: • Collect, organize, curate, and document healthcare information within the data warehouse • Apply experience with clinical information and workflows to the development of informatics tools, applications, analyses, and procedures • Develop, modify, test, and implement applications and algorithms for the collection, organization, and analysis of healthcare data • Assist in the development of presentations, scientific publications, and grant proposals • Apply insights gained from research to improve patient care or healthcare operations • Ability to interact directly with and interpret healthcare data using self-service tools or coding languages, such as SQL and Python • Ability to liaison between clinical stakeholders and Enterprise Data & AI technical team members • Expertise in analyzing and optimizing clinical workflows, leveraging IT to enhance efficiency, accuracy, and patient outcomes through targeted interventions and system improvements • Collaborate with software vendors and IT service providers to ensure that their products and services are tailored to meet the unique operational needs of the healthcare facility, optimizing performance and compliance • Other duties as assigned ***While there isn't a fixed requirement for weekly onsite days, candidates should ideally be available to come onsite one day a week, if needed.*** **Only those lawfully authorized to work in the designated country associated with the position will be considered.** **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client's business needs and requirements.** Benefits: For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website. California Pay Equity: For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here. Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances. If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department. Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).

Zachary Piper Solutions is seeking a Clinical Research Coordinator to join a site located in Newport Beach, California. The Clinical Research Coordinator will work On-Site 5 days a week. This job opens for applications on 01/07/2025. Applications for this job will be accepted for at least 30 days from the posting date. Responsibilities of the Clinical Research Coordinator include:·Assisting PI in screening and review of study participants eligibility·Maintaining case report forms, charts and documentation·Collect and entering data as necessary·Mentoring, training and high-level oversight of other clinical research coordinators and research assistants·Assist with study start-up, maintenance, and close-out of studies as needed for those on the team Qualifications for the Clinical Research Coordinator include:·1-2 years of experience in-roll as a Clinical Research Coordinator·Phlebotomy experience and current certification to preform phlebotomy in California·Completion of GCP Certification and advanced CRC preferred·Excellent verbal & written communication skills·Strong Interpersonal skills Compensation for the Clinical Research Coordinator:· Salary Range $25-$32/hr Depending on Experience· Full Comprehensive Benefits, Medical, Dental and Vision coverage Keywords:KEYWORDSClinical Research Coordinator, Clinical, Clinical Research, Clinical Trial Associate, CRO, Industry, Patient Recruitment, Site Support, TMF, Trial Master File ETMF, GCP, FDA,CRA, Clinical Research Training, Informed Consent, Healthcare, Health and Medical, Life Science, L-TH1, L-DNP, #Pando, CRF, Case Report Form, Trainer, M3, Data Entry, phlebotomy, blood draw,

The Encompass Group is partnering with a well-known hospital in the Orange County area that is looking to add an experienced Outpatient Clinic Coordinator to their growing team! The Outpatient Clinic Coordinator will provide a seamless experience for patients, efficient administrative processes, and adherence to clinic policies and procedures. The ideal candidate will be detail-oriented, organized, and passionate about providing excellent customer service in a healthcare setting. Responsibilities: Oversee day to day operations of the outpatient clinics, ensuring smooth functionality and timely service. Collect co-pays and other payments, providing clear explanations of charges and receipts. Verify patient benefits and eligibility prior to appointments, addressing any discrepancies or issues. Communicate benefit and coverage details to patients in a professional and understandable manner. Manage appointment schedules, ensuring efficiency and minimizing conflicts or delays. Maintain accurate patient records and ensure all necessary documentation is collected and stored appropriately. Work closely with clinical staff, billing teams, and management to ensure the clinic runs efficiently. Qualifications: 2 years of experience in a healthcare administrative or patient coordination role. Strong knowledge of insurance verification, benefits, and eligibility processes. Proficient in healthcare management software and Microsoft Office Suite. Comfortability in a ‘paper-free' work environment through use of technology Excellent organizational, multitasking, and problem-solving skills. Familiarity with HIPAA and other healthcare regulations.

Administrative Assistant, Clinical Coordinator Department: Clinical Hourly, Non Exempt- $24-$25/ hour InMode is a leading global provider of innovative medical technologies which develops, manufactures, and markets devices harnessing novel radiofrequency (RF) technology. The company strives to enable new emerging surgical procedures and improve existing treatments. By leveraging its medically accepted, minimally invasive RF technology for simultaneous subdermal adipose remodeling and skin tightening, InMode offers a comprehensive portfolio of products for plastic surgery, gynecology, dermatology, otolaryngology, and ophthalmology. Position Summary: The Clinical Coordinator will act as a liaison, provide product/services information and resolve any emerging problems with our customer accounts, sales representatives, and clinical trainers will assist with scheduling and organizing clinical training as well as provide other administrative support to the Clinical Department. The Clinical Coordinator will be organized, able to multi-task, empathetic, and passionately communicative as well as a team player and people-oriented. He or she can be depended on to complete a task under minimal supervision and will be a quick learner. Duties and Responsibilities: Coordinate and Schedule North American clinical in-services, prepare correspondences, and document and manage client records and databases. Approve Clinical Trainers Invoices Assist the field Sales Representatives, Customers, and Independent Training Consultants with scheduling training and demonstrations. Assist with customer clinical inquiries. Review Customer Survey, and create customers training certificates: Preceptorships and In-Services. Attend staff clinical training, for new products and new trainers. Perform other related duties as assigned. Minimum Qualifications: Minimum of 2 years working experience with Customer Service-related functions. Intermediate knowledge of MS Office Suite, and advanced knowledge of MS Excel. Experience with SalesForce.com systems preferred. Ability to multitask, work well under pressure and meet deadlines.

Our client, a Fortune 500 Medical Device Company, has engaged GForce Life Sciences to provide an entry level Clinical Contracts Associate. Working under the direction of the manager or senior contract associate, the Clinical Contracts Associate provides technical assistance in negotiating, reviewing, and processing clinical study and research contracts and budgets. Understands key business drivers and corporate clinical priorities; uses this understanding to accomplish own work. No supervisory responsibilities. Solves problems in straightforward situations; analyzes possible solutions using technical experience, judgment and precedents. Impacts quality of own work and the work of others on the team; works within guidelines and policies. Explains complex information to others in straightforward situations. Capable of negotiations with some supervision. Job Duties · Creating and negotiating Amendments · Preparing study-site specific budget drafts · Sending initial contract/budget email to invited sites within specified timelines · Periodic follow up with sites · Submitting finalized contracts for signatures · Scanning of fully executed contracts and revised Investigator agreements · Uploading of documents to electronic trial master file system and maintaining status notes · Attending calls and providing regular status updates as required · Filing of hard copy contracts · Preparing NTA agreement templates and sending out to sites · Licensing requests · Supporting Contracts Manager & Associates as required on assigned tasks Mandatory Requirements · Minimum of 1-3 years related work experience in clinical research · Associate's or Bachelor's Degree in Business Administration, a related field, or equivalent. · Negotiations/Skills in redlining documents and analytical experience or equivalent. · Familiarity with grant and contract requirements, policies, and procedures including, but not limited to: · Clinical and AdvaMed Code of Ethics on Interactions with Health Care Professionals. · Knowledge and understanding of GCP, ICH, GLP and other federal, state, industry rules and regulations governing technical aspects of clinical grants and contracts · Ensure all required data from studies and sites to comply with regulatory and government requirements (Sunshine Act, FWA, Human Subject Protection training, Clinical Insurance). · Sponsor Pharma or Biotech experience preferred. · Direct knowledge of Sponsor Clinical contracting preferred Term & Start · 9+ month contract with potential to extend · Based out of Sylmar, CA or Maple Grove, MN. · Preferred 3-4 days onsite with flexibility. · Benefits available (Medical, Dental, Vision, 401k)

Metro Infectious Disease Consultants is recruiting ambitious, infectious disease clinicians for openings within their Thousand Oaks, California locations. Primary responsibilities will include outpatient and inpatient ID consultations, outpatient antibiotic therapy, HIV medicine, and infection control. As a member of the largest ID private practice in the country we can offer a stimulating, balanced ID practice with a comfortable call schedule and lifestyle. Applicants must be board certified or eligible in Infectious Diseases. Please fax or e-mail your CV to: Tara Kowalski Human Resources E-mail - tkowalski@midcusa. com Fax- 630-734-4685

Expand Show Other Jobs Job Saved Research Coordinator - CHAMP Clinic UCLA Details **Posted:** 06-Dec-24 **Categories:** Academic / Research **Description**The Semel Insititute is seeking a part time Assistant Clinical Research Coordinator to provide research support for the Child & Adolescent Bipolar Mood Disorders Program (CHAMP) in the Semel Institute's Child and Adolescent Psychiatry Division. Major functions include screening potential study participants, scheduling, consenting, and completing assessments for the research programs being conducted in the clinic, as well as basic administrative duties relevant to this research (faxing, coping, coordination with providers, data entry). The person will be working to set up and run a newly funded study- "A Ketogenic Diet Approach to Bipolar Disorder in Adolescents"- which is a 2 year, multi-site study of adolescents and young adults with bipolar disorder. In this role you will be responsible for participant recruitment, consenting, managing participant follow up appointments, scheduling of interviews, and reliability checks. In addition you will also meet regularly with coordinators of other research sites to ensure consistency between teams, organize research data, and provide updated reports to investigators at bi-weekly all site meetings. Pay Range: $27.08 - $43.55 hourly **Qualifications**Required: * Minimum of 1+ years of experience in a clinical research setting * Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as member of a team. * Ability to effectively communicate to and interact with patients in a compassionate and kind manner. * Ability to set priorities and complete ongoing tasks with competing deadlines, with frequent interruptions, to meet the programmatic and department needs, while complying * with applicable University policies and federal and state regulations. * Analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective actions. * Close attention to detail to ensure accuracy in a fast-paced, fluctuating workload environment. * Organization skills to create and maintain administrative and regulatory files effectively as well as independently balance the various tasks to ensure deadlines are met. * Demonstrated proficiency with Adobe and Microsoft suite software, especially Excel, to perform daily tasks efficiently and accurately. * A learning and professional growth mentality so that new software tools, systems, and processes can be adopted quickly and efficiently. * Working knowledge of clinical research concepts, policies and procedures, and human safety protection regulations and laws. * Knowledge of and experience working with a variety of local and external IRBs, scientific review and other research committees, national cooperative group sponsors, industry sponsors, federal and foundation funding organizations, etc. * Strong verbal and written communication skills to effectively establish rapport, building collaborative relationships, and communicate complex concepts and ideas in an easy-to- understand manner * Ability to adapt to changing job demands and priorities, remain flexible including working flexible hours to accommodate research deadlines. * Ability to handle confidential information with judgement and discretion. * High degree of concentration and focus in a work environment that contains distracting stimuli, competing deadlines, and work delegated by more than one individual. * Availability to work in more than one environment, travelling to various clinic sites, meetings, conferences, etc. Preferred: * Bachelor's degree About At UCLA Health, you can help heal humankind, one patient at a time by improving health, alleviating suffering and delivering acts of kindness. As you do, you'll achieve great things in your life and your career. We're a world-class health organization with four hospitals consistently recognized among the nation's very best as well as an internationally-renowned medical school, primary and specialty care clinics and much more. Within our dynamic, innovative and growing organization, you'll find exceptional opportunities to make the most of your abilities in a supportive, empowering and inclusive environment. If you embrace our values of Integrity, Compassion, Respect, Teamwork, Excellence and Discovery we invite you to see all you can accomplish at UCLA Health.

About Us: Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k. Schedule: Monday - Friday (08:00am - 4:30pm) Hourly Range: $29.00 - $34.00 (Depending on Experience) Job Summary: Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies. Essential Responsibilities and Duties: Assists with coordinating all aspects of patient involvement from study initiation until study completion. Organizes research information for clinical trials. Observes subjects and assists with data analysis and reporting. Schedules the collection of data. Documents adverse events, protocol deviations, and other unanticipated problems appropriately. Reports research data to maintain quality and compliance. Performs administrative and regulatory duties related to the study as appropriate. Participates in other protocol development activities. Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.) Educates potential participants and caregivers on protocol specific details and expectations. Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned). Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive. Education/Experience/Skills: High school graduate or equivalent; Bachelor's Degree, preferred. 1+ years of experience as a Clinical Research Coordinator or similarly responsible position (Required) Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials. Strong leadership and mentorship skills. Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level. Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations. Works independently as well as functioning as part of a team. Must be able to effectively communicate verbally and in writing. Working Conditions Indoor, Office environment. Shift work, depending on location. Essential physical requirements include sitting, typing, standing, and walking. Lightly active position, occasional lifting of up to 20 pounds. Rarely lift over 20 pounds. Reporting to work, as scheduled, is essential. Overnight travel may be required for training and/or investigative meetings. CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.

Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team! This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a competitive salary. WE OFFER THE FOLLOWING * Competitive travel bonus; * Equity/Stock Option program; * Training completion and retention bonus * Annual merit increases; * 401K matching; * The opportunity to work from home; * Flexible work hours across days within a week; * Retain airline reward miles and hotel reward points; * Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere; * In-house travel agents, reimbursement for airline club, and TSA pre-check; * Opportunity for leadership positions - Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager, and many more; * CRA training program (PACE); * Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts; * In-house administrative support for all levels of CRAs; and * Opportunities to work with international team of CRAs. Responsibilities * Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; * Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; * Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; * Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; * On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; * Verification that the investigator is enrolling only eligible subjects; * Regulatory document review; * Medical device and/or investigational product/drug accountability and inventory; * Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; * Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement; and * Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. Qualifications * Must have a minimum of a Bachelor's degree in a health or science related field; * Experience as a Clinical Research Coordinator (minimum 1 year); * Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely; * Must maintain a valid driver's license and the ability to drive to monitoring sites; * Proficient knowledge of Microsoft Office; * Strong communication and presentation skills; and * Must be detail-oriented and efficient in time management. Compensation A target salary range of $70,000 - $160,000. Your compensation will be based on your skills and experience. Medpace offers the following benefits for eligible positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, and pet insurance. For more details, please discuss with your recruiter. #LI-Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks * Flexible work environment * Competitive PTO packages - starting at 20+ days * Company-sponsored employee appreciation events * Employee health and wellness initiatives * Competitive compensation and benefits package * Structured career paths with opportunities for professional growth * Discounts for local businesses Awards * Named a Top Workplace in 2024 by The Cincinnati Enquirer * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets

Description and Requirements JOB STATUS: Full-time WORK SCHEDULE: Mon - Fri Moderators are expected to interact directly with study participants using provided study protocols and managing the data collected during each session. Moderators will report to the Project Manager and Project Coordinator. Training will be provided before the start of data collection. Sessions occur onsite in Los Angeles, CA, with additional support staff on-site to manage participant intake and provide technical support. Main Responsibilities * Receive participants at work and guide them through the video study in a controlled environment * Ensure all recordings are done per project guidelines and upload the data * Have all participants complete a survey at the end of each session * Follow COVID-19 sanitization procedures after each session * Represent and promote the TELUS AI brand Minimum Requirements * Technical/troubleshooting skills; address fundamental problems with launching apps and uploading data * Familiarity with iOS and Mac OS * Experience with data collection and data management * Experience with video recording * Able to commit to a weekly schedule for the duration of the project * Ability to interact professionally with project participants * Experience with progress tracking and reporting, comfortable with Excel or Sheets Rate: $33.00 per hour TELUS International Values: TELUS International recognizes and embraces the importance of values in our ever-changing workplace. To be successful, all applicants must demonstrate behaviors that are reflective of our values: * We embrace change and initiate opportunity * We have a passion for growth * We believe in spirited teamwork * We have the courage to innovate At TELUS International, we are committed to diversity and equitable access to employment opportunities based on ability. Additional Job Description Moderators are expected to interact directly with study participants using provided study protocols and managing the data collected during each session. Moderators will report to the Project Manager and Project Coordinator. Training will be provided before the start of data collection. Sessions occur onsite in Sunnyvale, CA, with additional support staff on-site to manage participant intake and provide technical support. EEO Statement At TELUS Digital, we enable customer experience innovation through spirited teamwork, agile thinking, and a caring culture that puts customers first. TELUS Digital is the global arm of TELUS Corporation, one of the largest telecommunications service providers in Canada. We deliver contact center and business process outsourcing (BPO) solutions to some of the world's largest corporations in the consumer electronics, finance, telecommunications and utilities sectors. With global call center delivery capabilities, our multi-shore, multi-language programs offer safe, secure infrastructure, value-based pricing, skills-based resources and exceptional customer service - all backed by TELUS, our multi-billion dollar telecommunications parent. Equal Opportunity Employer At TELUS Digital, we are proud to be an equal opportunity employer and are committed to creating a diverse and inclusive workplace. All aspects of employment, including the decision to hire and promote, are based on applicants' qualifications, merits, competence and performance without regard to any characteristic related to diversity.

Irvine Clinical Research is the largest independent clinical trial group on the West Coast. Most of our research is in neurology (Alzheimer's Disease treatment and prevention studies); we also conduct trials in psychiatry and obesity medicine. In this role, we are seeking CRCs with proven trial experience. Ideally, candidates will have worked as a primary coordinator on a high-enrolling and/or highly complex drug trial and produced quality work.Job Duties Manage daily operations for assigned clinical trial projects Perform study procedures in accordance with GCP and study protocols Organize and maintain paper and electronic study data in a complete and correct manner Cultivate enthusiastic and professional relationships with patients and sponsors alike Work closely with recruitment and prescreening teams to meet study enrollment goals Conduct diagnostic, efficacy, and safety assessments as needed Job Requirements Two (2) or more years of clinical research coordinator experience Attention to detail and the ability to handle multiple tasks with precision Demonstrated ability to work accurately and quickly with CTMS A command of professional spoken and written English $66,560 - $80,000 a year Hours and CompensationThis is a full-time employment position based in-person at our clinic in the Alzheimer's Orange County building in Irvine or at one of our other network sites in Los Angeles and Riverside Counties. Training will be at our flagship site in Irvine. The estimated salary for this position is between $62k-$80k per year, depending on experience and education. The company pays for 100% of health/dental/vision individual insurance costs for eligible full-time employees. Vacation (PTO) is earned at a rate of 3 weeks per year.

The Clinical Research Coordinator II conducts and manages multiple clinical trials from start-up through study close-out in accordance with the study protocol, GCP, and SOPs. This role involves implementing and coordinating clinical trials, managing vendor relationships, recruiting subjects, and ensuring all regulatory requirements are met. Responsibilities * Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and SOPs. * Implement and coordinate assigned clinical trials including start-up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, and ensuring data is entered in a timely manner. * Resolve all queries, manage and report adverse events, serious adverse events, and deviations, implement new protocol amendments, and provide all close-out activities. * Develop, coordinate, and implement research and administrative strategies to successfully manage assigned protocols. * Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors. * Apply good documentation practices when collecting and correcting data, transferring data to sponsor/CRO data capture systems, and resolving queries. * Maintain confidentiality of patient protected health information, sponsor confidential information, and proprietary information. * Verify and escalate patient safety concerns by ensuring all adverse events, serious adverse events, and adverse events of special interest are followed and reported in accordance with the protocol and SOPs. * Ensure all data is entered into the sponsor's data portal and all queries are resolved in a timely manner. * Ensure staff are delegated and trained appropriately and documented. * Create, collect, and submit regulatory documents to sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements. * Evaluate potential subjects for participation in clinical trials including phone and in-person pre-screens. * Create and execute recruitment strategies defined by the team. * Understand key timelines, endpoints, required vendors, and patient population for each assigned protocol. * Understand the product development life cycle and significance of protocol design including critical data points. * Understand the disease process or condition under study. * Collaborate to develop a Quality Control strategy for reviewing work on an ongoing basis and in preparation for monitor visits. * Perform clinical duties (e.g., drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope. Essential Skills * Experience with clinical trials and research. * Proficiency in pre-screening patients and obtaining consent. * Bilingual capabilities. * Phlebotomy skills. * Clinical research experience. * Experience with electronic data capture (EDC) systems. Additional Skills & Qualifications * Bachelor's degree and 2 years relevant experience in the life science industry OR * Associate's degree with 4 years relevant experience in the life science industry OR * High School Graduate and/or technical degree with a minimum of 6 years relevant experience in the life science industry AND * 1 year Clinical Research Coordinator experience. Work Environment This position is onsite and offers private examination/consultation rooms, comfortable patient reception areas, facilities for extended-stay pharmacokinetic studies, parking, a nursing station, secure monitoring rooms or workstations with phone & high-speed internet access, multiple individual & secure workstations for research staff, a regulatory document processing area, and electronic data capture capabilities. The facility also includes secure record storage, a CLIA certified research laboratory or clinical laboratory with a CLIA waiver, ambient and refrigerated centrifuge, secured & temperature-controlled investigational product storage with pharmaceutical refrigerator & freezer, freezers equipped for laboratory specimens at -20 & -70 degrees Celsius, a backup generator/power source in the event of site power loss, and standard medical equipment, including ECG machines, digital and analog scales. Pay and Benefits The pay range for this position is $64400.00 - $72800.00 Health and Wellness Benefits Medical, dental, vision, HSA, and FSA plans Employer contributions from 55-80% based on coverage level Company contributions to HSAs 401k Eligibility and Company Match 100% match of the first 3% of contributions; 50% on the next 2% contributed Immediate eligibility and automatic enrollment at 5% contribution Paid Time Off and Company Holidays PTO starting at three weeks per year and growing with company tenure 10 paid holidays each calendar year Life Insurance and Employee Assistance Program 100% paid life Insurance policy (double annual salary) 100% paid short- and long-term disability benefits Optional insurance coverage for the employee and dependents Complimentary emergency assistance plan Site Incentive Bonus Plan Site bonuses are paid twice annually Ties site team success to Velocity's success Recognition and reward for individual contributions Workplace Type This is a fully onsite position in Gardena,CA. Application Deadline This position will be accepting applications until Jan 29, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job | Aug 09, 2024 | Medicine Sign up with scientific.today to see **all content** and to create a **personalized stream** of news, jobs and events, by defining keywords and following your favorite content sources. Join Parexel's team of changemakers as we help advance healthcare throughout the globe, all while keeping the patient at the heart of everything we do. **Job Title:** Clinical Research Coordinator **Job Introduction:** As a Clinical Research Coordinator, you will execute and coordinate a variety of specialized clinical research activities within the Early Phase Clinical Unit (EPCU), ensuring that assigned protocols are executed with high quality, and Standard Operating Procedures (SOPs)and GCP/ICH guidelines are followed. Primary responsibilities for assigned trials include development of clinical execution strategies, management of source data collection and coordination of core study team (medical, pharmacy, laboratory, enrollment). **Who we're looking for:** We are looking for a motivated problem solver with proven experience leading and coordinating clinical trials in a fast-paced environment with a passion for working in clinical research. **What you'll do (including but not limited to):** * Review and understand the study protocol, proactively seeking to identify and address questions and operational risks with Project Manager and/or sponsor to ensure successful execution of studies * Responsible for study resource allocation, maintaining timely resource requests and optimizing efficient and effective planning and utilization of resources. * Responsible for ensuring study team training compliance with protocol and any other study procedure/task required trainings, arranging and providing trainings as appropriate to ensure study team members are oriented and understand tasks to be performed. * Responsible for establishing and ensuring timelines relating to area of responsibility are met. * Responsible for data quality and protocol compliance excellence demonstrated in study start up, execution, and closeout through accuracy in ClinBase or paper source, ensuring source data entry completeness and adherence to GCP, meeting study timelines. * Responsible for ensuring procedure coverage and task execution, coordinating with other departments to optimize efficiency in execution. * Responsible for creating study specific paperwork and or materials as needed. * Communicates with physicians and relevant Clinical Staff in evaluating study participant status. * Responsible for monitoring study participant test results, including but not limited to Adverse Events, laboratory, vitals, ECG, and other procedure results, escalating any protocol, safety or other concerns as appropriate to medical group and management. * Responsible for oversight with monitors, proactively seeking to ensure preparation for the visit with study materials, establishing study team presence and coverage, to expedite and address query, question and or issue resolution as soon as possible. * Responsible for overseeing clinical trial volunteers according to protocol specific requirements and CFR/ICH GCP guidelines. Ensure all study laboratory and medical tests are completed and the eligibility requirements specific to assigned studies are met. * Oversee study data entry and QC, ensuring sponsor timelines are upheld through timely data entry, query resolution, and data transfers, communicating updates to PM. * Oversees study team to ensure Glendale Medical Adventist Center (GAMC) subject requirements for dietary, admission and safety are collected and provided to GAMC in a timely manner. * Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and is not to be considered as all inclusive. **Additional details:** * Clinical Research Coordinator experience required * Experience working on early phase trials preferably at the site level * Preferred knowledge of the following systems: VeevaVault and Medidata * Proven capability to work in a fast-paced environment with effective time management of multiple tasks and prioritizing workload as needed * Bachelor's or Master's degree in health sciences highly preferred or applicable experience * Ability to work onsite in Glendale, CA M-F (occasional weekends might be required) Base Pay Range: $28.00 to $33.00 per hour Actual salaries may vary within the range based on several factors including, but not limited to education, training, experience, professional achievement, and location. In addition to base salary, some roles may be eligible for participation in Parexel's annual performance-based bonus plan, annual salary review and additional total rewards incentives. Our talent acquisition team will provide additional details on our bonus plan or incentive programs for those eligible roles. For all eligible employees, we offer market leading benefit programs including paid time off, 401k match, life insurance, health insurance, and other benefit offerings in accordance with the terms of applicable plans. **Why join us:** Be part of groundbreaking projects that are pushing the boundaries of the industry. Experience a collaborative and inclusive work environment that highly appreciates your expertise. Unlock your full potential with professional growth and development opportunities. Enjoy work life balance and flexible working hours. **Parexel US Benefits:** Health, Vision & Dental Insurance Tuition Reimbursement Vacation/Holiday/Sick Time Flexible Spending & Health Savings Accounts Work/Life Balance 401(k) with Company match Pet Insurance Full list of benefits available here: If this job doesn't sound like the next step in your career, but perhaps you know of someone who'd be a perfect fit, send them the link to apply! Parexel is dedicated to supporting, developing, and retaining a diverse workforce, inclusive of veteran and military spouse talent. The skills and values you have developed are transferrable to meaningful careers at Parexel.” Originaly published: July 31, 2024, 8:31 a.m. with scientific.today to create a **personalized stream** of news, jobs and events, by defining keywords and following your favorite content sources. If you already have an scientific.today, Facebook or Google account: Edit rights: to post comments. **Comments** There are no comments yet. **Read also** None | News None | News Immunology | News Astrophysics | News