Clinical Research Coordinator Jobs in Stockton, CA

W2 Contract Salary Range: $156,000 - $176,800 per year As a Senior Clinical Trial Manager with expertise in oncology drug development, you will be responsible for Contract Research Organization (CRO) oversight and execution of clinical studies. We require a clinical operations professional with technical expertise in managing Phase I-III clinical trials in an industry setting and a strong knowledge of clinical operations, Good Clinical Practice (GCP), and U.S. Food and Drug Administration (FDA) regulatory requirements. Duties and Responsibilities: Perform clinical operations functional activities related to the execution of assigned clinical trials based on department and corporate goals and objectives. Manage clinical studies and vendors to ensure studies are completed on time, within budget, and in compliance with Standard Operating Procedures (SOPs), FDA regulations, and International Council for Harmonization (ICH)/ GCP guidelines. Identify, engage, and manage the activities of clinical CROs and other clinical study providers (e.g., core labs, Electronic Data Capture (EDC) providers, and independent contractors) to execute clinical trials. Review and contribute to developing study-specific documentation, including clinical trial protocols, case report forms, study guides/manuals, informed consent forms, and clinical databases. Review monitoring reports and other study documentation as required. Oversee the collection and management of clinical trial documentation to be filed in the Trial Master File (TMF). Participate in team meetings and collaborate with other functional groups within the company (e.g., Clinical Development, Pharmacokinetics, Quantitative Sciences, Regulatory, QA, Finance, Legal, etc.) to achieve clinical study goals. Follow up on assigned team action items and identify, escalate, and resolve issues as needed. Collaborate with contracts specialists to review and negotiate Clinical Trial Agreements and site-specific study budgets. Assess the adequacy and feasibility of potential clinical investigators and sites, including evaluating facilities, personnel, patient referral base, and adherence to GCP. Develop clinical study monitoring priorities and Monitoring Plan in conjunction with CRO. Conduct site visits (e.g., training visits, site initiation visits, monitoring visits) as required. Manage investigational product accountability and reconciliation process. Assist with preparing safety, interim, and final clinical study reports and resolving data discrepancies. Provide clinical trial support, mentoring, leadership, guidance, and direction to Clinical Research Associates (CRAs) assigned to clinical studies. Prepare and track study participant enrollment projections vs. actuals and study budgets. Serve as a primary clinical operations contact for internal and external (clinical sites, vendors, etc.) teams for assigned studies. Requirements and Qualifications: BS or MS degree with at least 6+ years of clinical operations experience in oncology drug development Hands-on experience running early-stage clinical trials within an industry environment Strong working knowledge of FDA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials Experience in selecting CROs and vendors and managing external resources. A demonstrable record of strong vendor management and teamwork Direct experience managing clinical CROs Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high-energy environment. Excellent written and verbal communication skills Able to multi-task, prioritize options, anticipate challenges, and execute goals as a member of an interdisciplinary team Able to travel (~25%). Experience working with cooperative group studies and investigator-sponsored trials is preferred. Experience in global clinical trial operations is desirable. Knowledge of APAC regulations is highly desired. Desired Skills and Experience Oncology drug development, Phase I-III clinical trials, GCP, FDA regulations, ICH guidelines, contract research organization, vendor management, travel Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as a W2 candidate. Bayside Solutions, Inc. may collect your personal information during the position application process. Please reference Bayside Solutions, Inc.'s CCPA Privacy Policy at *************************

Meet has partnered with one of our top biotech clients in the bay area. They are seeking a seasoned Senior Clinical Research Associate to join their growing team. As a Senior Clinical Research Associate, you will play a crucial role in the planning, execution, and monitoring of medium and large-sized clinical trials. You will ensure that studies are conducted in accordance with regulatory requirements, Good Clinical Practice (GCP), and company policies. This is a significant opportunity to progress therapeutics for metabolic and oncologic conditions. Responsibilities: Study Management: Assist in the design and implementation of clinical study protocols, case report forms, and informed consent documents. Work closely with Study Lead across projects Site Monitoring: Conduct regular site visits to ensure compliance with study protocols, GCP, and regulatory requirements. Monitor patient recruitment and retention. Data Collection & Management: Review and verify data quality and accuracy. Assist in data entry and maintenance of clinical databases. Ensure Trial Master File is maintained. Regulatory Compliance: Ensure that all clinical trials are conducted in compliance with local, national, and international regulations. Prepare documentation for regulatory submissions and audits. Collaboration: Work closely with investigators, site staff, and cross-functional teams to facilitate smooth study operations and resolve any issues that arise. Partner with CMC team for drug supply forecasting Training: Provide training and support to site staff on study protocols, procedures, and data collection methods. Reporting: Prepare regular progress reports and communicate findings to project teams and management. Requirements: BS/BA in relevant discipline and at least 4 years of industry experience working across clinical research functions - ideally managing most aspects of clinical studies Experienced as a CRA ideally for a Sponsor company and ideally in a CRO or a CRA/field monitor environment Understanding of clinical trials process, SOPs, medical terminology, and US and GCP/ICH regulations Excellent written and verbal communication Contact: Please reach out to Payton Baker at ************ or ********************************* to learn more. Correspondence will be confidential.

Program Operations Manager / Research Coordinator Sutherland Labs is an international team of researchers, designers and creatives who work with leading brands to improve everyday experiences. A small but mighty design research practice in San Francisco looking for an Operations innovator with research chops to join our smart, creative and warm team. If running a remote diary study in two languages; executing a field study in a major city with wearable technology; or delivering on a multi-country recruiting strategy sounds like a thrilling challenge, we hope you'll get in touch. RESPONSIBILITIES: A. Program Operations: Create, optimize and roll out processes and a toolkit to support our researchers, in collaboration with other team members. An innovative mindset and ability to get the most out of Monday, Dovetail and similar platforms is highly desirable. Act as a key liaison between project teams and our business manager, delivering a seamless experience for clients during the sales and contracting phase of engagements, while ensuring that legal, compliance and finance requirements are met on a timely basis. Maintain our processes and Knowledge System, and contribute to the development of documentation to aid the organization of research activities. Liaise with recruiters and project leads to ensure participant recruitment is on time and to budget. Coordinate multi-track recruiting strategies, including guerrilla methods and user research platforms, as necessary. Directly communicate, follow up with, or schedule research participants when necessary. Assist the process of estimating costs, writing proposals and drafting contracts. Play a key role in managing the production, review, execution and delivery of documents. Reconcile and process invoices to clients and for vendors. Help identify and vet suitable vendors and suppliers for all our research needs - from recruiters to local informants, to technology vendors. Help position us to stay on the leading edge of research innovation through vendor relationships. Oversee vendor relationships, from sourcing to onboarding, through to signing off on invoices. Manage resource plans and calendars. Monitor project expenditures and highlight savings opportunities. Help create support materials and develop a trauma-informed, accessible and human-centric experience for research participants and our staff through all aspects of their engagement with Sutherland Labs. Coordinate and analyze participant feedback on their experience. Ensure compliance with data protection requirements throughout the course of client engagements. Support hiring, onboarding and offboarding processes for research team members. Coordinate team-building activities. B. Research Coordinator: Manage asynchronous data collection activities, e.g. diary studies and unmoderated research exercises, including participation in the planning and execution of analysis. Manage the sourcing, coordination and production of digital and physical research deliverables, including video production operations (editing skills not required), production of workshop materials, and research stimulus. Participate in research sessions and workshops as a technical concierge, co-facilitator, or note-taker. Help organize research notes, recordings, and other artefacts. Support in-context research and in-person workshops as a concierge, scout, or site coordinator. QUALIFICATIONS: Bachelor's Degree; however exceptional candidates may instead have experience that serves as an equivalent. 3+ years of Research Ops experience; or a strong point of view on how your experience would contribute. Entry level or early career qualitative research experience is a plus; enthusiasm for the research craft is essential. An eye for detail, exemplary organizational skills, and a drive to continually improve operational processes. A willingness to get scrappy and roll up your sleeves on occasion (We're a small, warm team who are passionate about our work). We are pleased to offer our team a time-off-in-lieu benefit in recognition that we occasionally work extended hours Strong verbal, written, and communication skills. Additional information: Role is hybrid - Must be based in the San Francisco Bay Area and able to attend our offices in downtown San Francisco at least 2 days a week

Coordinate and manage clinical trials to ensure compliance with protocols, regulations, and institutional policies, supporting participant safety and study integrity. Key Responsibilities: Facilitate site initiation and sponsor-required training for clinical protocols. Dispense study medications and coordinate with pharmacy staff as needed. Process and ship lab specimens in compliance with federal regulations. Conduct informed consent processes, ensuring proper documentation and compliance. Schedule and oversee study visits, tests, and procedures per protocol requirements. Accurately collect and report data, maintaining research subject charts and source documents. Perform or coordinate clinical procedures (e.g., blood draws, ECGs) with appropriate training. Report adverse events, protocol deviations, and violations to study sponsors and IRBs. Prepare and submit regulatory documents, including IRB applications and consent forms. Support participant recruitment, screening, enrollment, and retention. Serve as a liaison between participants, investigators, sponsors, and regulatory bodies. Assist in sponsor monitoring visits and audits, resolving findings promptly. Qualifications: 4+ years as a Clinical Research Coordinator Oncology experience required Phlebotomy Certification preferred Knowledge of clinical research protocols, GCP, and FDA regulations. Strong organizational, communication, and multitasking skills. Experience with clinical procedures and data management preferred. Details: Location: Sacramento, CA Pay: $35/hr-$50/hr (Dependent on background and years of experience) Hours: Monday - Friday; Normal Business Hours; Onsite 5 Days a Week Duration: Contract to Hire (1040 Hours)

Job Title: Clinical Research Coordinator I - Cardiovascular Research 12-month contract About the Role: We are seeking 2-3 Clinical Research Coordinators (CRC I) to join our cardiovascular research team. This entry-level role is ideal for individuals passionate about clinical research and patient care, looking to make an impact in advancing cardiovascular health. The position will primarily be based onsite at our Oakland and Pleasanton clinics, supporting our ongoing clinical trials and studies. Key Responsibilities: Participant Recruitment: Conduct phone screening to recruit eligible patients and members for cardiovascular studies. Informed Consent: Obtain and document informed consent from study participants, ensuring understanding and compliance with study protocols. Clinical Measurements: Collect and record physical metrics, including height and weight, during participant visits. Data Entry: Maintain accurate and timely entry of study data into electronic databases and research systems. Follow-Up Coordination: Schedule and conduct participant follow-ups, addressing any questions or concerns regarding the study. Regulatory Compliance: Ensure adherence to study protocols, regulatory requirements, and ethical guidelines at all times. Qualifications: Bachelor's degree in health sciences, biology, public health, or a related field (preferred but not required with relevant experience). Strong interest in clinical research and patient interaction. Excellent organizational skills and attention to detail for accurate data entry and record-keeping. Ability to effectively communicate with patients, research team members, and study sponsors. Previous experience in a healthcare or research setting is a plus. Work Environment: This position requires onsite work at both the Oakland Clinic and Pleasanton location. Reliable transportation to travel between clinic sites is essential.

Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities Participate and assist in design and preparation of protocols and case report forms. Generate clinical SOPs, policies, charters, and plans according to US and international guidelines. Participate in the evaluation of potential clinical sites according to established criteria of acceptability. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials. Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Prepare site visit reports with identification of key accomplishments, key issues for resolution and recommendations for follow-up actions for assigned study sites. Conduct study termination visits, obtain final reports from investigators, and participate in the preparation of final reports for regulatory submission. Assist with the maintenance of clinical archive and electronic files. Other tasks as assigned. Requirements To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. BA, BS, RN, BSN or equivalent Basic knowledge and adherence to GCPs 1-2 years of clinical research experience or equivalent experience or training Strong attention to detail Ability to multi-task Unquestionable integrity and highest ethical standards Excellent written and verbal communication skills Self-motivated, assertive, and driven BenefitsDental, Medical, Vision and 401K

As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. + Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. + Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. + Collaborating with investigators and site staff to facilitate smooth study conduct. + Performing data review and resolution of queries to maintain high-quality clinical data. + Contributing to the preparation and review of study documentation, including protocols and clinical study reports + Bachelor's degree in a scientific or healthcare-related field highly preferred. + Minimum of 2 years of experience as a Clinical Research Associate (on site monitoring experience required) + In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. + Strong organizational and communication skills, with attention to detail. + Ability to work independently and collaboratively in a fast-paced environment. **What ICON can offer you:** Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: + Various annual leave entitlements + A range of health insurance offerings to suit you and your family's needs + Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead + Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being + Life assurance + Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: ************************************ At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we've done to become a more inclusive organisation. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. ***************************************************** Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.

Job Title: Clinical Research Associate Job Contract Type: Full-time Job Seniority Level: Mid-Senior level More than one million people in the United States today are fighting blood cancer. While a traditional allogeneic stem cell transplant has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks. With our purified, high-precision investigational cell therapies we hope to not only replace patients' blood and immune systems with healthy ones, but also restore their lives. Summary: In this contract CRA role, you will be responsible for monitoring the progress of clinical studies (primarily, our phase 3 Precision-T study), either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements. You can be based anywhere in the U.S., although west coast is preferred. Travel expected: :1+ site visit per week, for sites that do not permit virtual monitoring. Responsibilities: Conduct interim monitoring visits (IMVs) and ISF review Review electronic medical records (EMR)/patient data Source documentation verification (SDV) 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 Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol Provide support to site staff including research coordinators and physicians Assist in the development of trial materials as needed (e.g., case report forms, monitoring guidelines, site tools and training guides) Contribute to the development of Clinical Operations SOPs, best practices, work instructions, tools and templates Desired Qualifications: BA/BS or equivalent with a minimum of 3+ years of relevant clinical trial management experience Therapeutic experience in oncology/hematology and cell and gene therapy preferred Prior CRA experience working directly for sponsor, ideally a start-up/or small company, in a co-monitoring capacity Strong working knowledge of FDA and ICH/GCP regulations and guidelines and thorough knowledge of clinical monitoring procedures Experience with Trial Master File management according to the DIA reference model Experience operating within various site EMR/EHR systems Experience using eTMF, EDC (IBM Zelta experience ideal), CTMS, and other vendors systems/portals Personal Qualities: Highly detail oriented with special attention to quality and quality control Ability to multitask and handle multiple responsibilities simultaneously; able to prioritize Well organized and able to work under tight deadlines Demonstrated strong work ethic, curiosity to learn and contribute in a fast-paced collaborative environment Strong interpersonal skills, including verbal and written communication, are essential Ability to work in a collegial and collaborative manner; independently and as part of a team Ability to work in a fast-paced and informal startup environment Highly tolerant and respectful of all members of our team Strong problem-solving skills with desire to improve upon established processes Sense of humor Who We Are We are driven by a passion for science and compassion for patients. We act with urgency to ensure our treatments are one day accessible to all who need them. We live by our core values of passion, courage, and integrity. Excellence in our work means the chance to unlock a better quality of life for our patients, and with that comes tremendous responsibility. We innovate on a path that hasn't been paved. We embrace an entrepreneurial spirit and take calculated risks to achieve our mission. We aren't afraid to ask “why not” and challenge the status quo. We maintain a start-up culture of camaraderie and leadership by example, regardless of title. We're proud to be an equal opportunity employer, and recognize that celebrating our differences creates stronger, lasting solutions that better serve our team, our patients and their healthcare providers. To learn more: ********************************** **all official communication will be *****************; please beware of scams** Notice to staffing firms Orca Bio does not accept resumes from staffing agencies with which we do not have a written agreement and specific engagement for a particular opening. Our employment activities, inquiries and offers are managed through our HR/Talent team, and all candidates are presented through this channel only. We do not accept unsolicited resumes, and we rarely outsource recruitment. Lifelancer ( ********************** ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. For more details and to find similar roles, please check out the below Lifelancer link. **********************/jobs/view/d04107404e4ad06601d**********65f

: We are creating the future of brain-computer interfaces: building devices now that have the potential to help people with paralysis regain mobility and independence and invent new technologies that could expand our abilities, our community, and our world. Team Description: The Clinical Team is responsible for the development, implementation, execution, and oversight of Neuralink's human clinical trial operations. We build and manage key relationships between internal Neuralink teams and external organizations such as study sites, research partners, regulatory bodies, and other entities essential to successfully carrying out human clinical trials. Job Description and Responsibilities: As a Clinical Research Associate, you'll play a crucial role in pioneering groundbreaking clinical studies! Your work will directly contribute to the planning, execution, and success of innovative trials, from the initial phases of study setup to hands-on clinical monitoring and site management. You'll be visiting sites both in-person and remotely to ensure protocol and regulatory compliance, tackle safety event management, and maintain essential documentation. Collaborating closely with a passionate, cross-functional team, as well as external partners, you'll be at the forefront of Neuralink's mission to push the boundaries of what's possible in clinical research. Additional job responsibilities will include: Conducting qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocols and applicable regulations Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff Verifying medical record and source documentation against case report form (CRF) data, including informing the site staff of any entry errors, ensuring good documentation (GDP) 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) to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward Assisting in regulatory document write-up and reviews Organizing and submitting IRB/EC submissions and applicable regulatory documentation with follow-through to ensure successful outcomes Amending clinical study documents (ICF, CRFs, Monitoring Plan, etc…) as needed and helping clinical sites with institutional review board submission as necessary Reviewing and verifying adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with protocol Assessing the clinical research site's patient recruitment and retention success and offering suggestions for improvement as well as helping with Sponsor recruitment activities Completing monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance Contributing to the review of consent form language for consistency across protocols Required Qualifications: Bachelor's degree in life sciences or related field Minimum of 5 years of experience working in clinical trials with 3 years as a Clinical Research Associate Strong understanding of GCP, FDA, and ICH guidelines, regulations, and compliance requirements (e.g., 21 CFR 812, ISO14155) Proven ability to manage multiple tasks, prioritize workload effectively, and meet deadlines in a fast-paced environment Excellent interpersonal, communication, and organizational skills Ability to travel domestically and internationally, as required, up to 50% Preferred Qualifications: Advanced degree in life sciences or related field Significant experience in medical device studies Certification as a Clinical Research Professional (CCRP) or equivalent Proficiency in Microsoft Office Suite and familiarity with electronic data capture (EDC) systems Experience working in a fast-paced medical device startup environment Experience working in neuromodulation, surgical robotics, or another Class III implantable device Pay Transparency: Based on California law, the following details are for California individuals only: California base salary range: $74,000—$113,000 USDFor Full-Time Employees, your compensation package will include two major components: salary and equity. Guidance on salary for this role will be determined according to the level at which you enter the organization, with the ability to gain more over time as you contribute. In addition, Full-Time Employees are eligible for the following benefits listed below. What We Offer: An opportunity to change the world and work with some of the smartest and most talented experts from different fields Growth potential; we rapidly advance team members who have an outsized impact Excellent medical, dental, and vision insurance through a PPO plan Paid holidays Commuter benefits Meals provided Equity + 401(k) plan *Temporary Employees & Interns excluded Parental leave *Temporary Employees & Interns excluded Flexible time off *Temporary Employees & Interns excluded

About Us : How many companies can say they've been in business for over 17 7 years?! Here at ZEISS , we certainly can! As the pioneers of science , ZEISS handles the everchanging environment s in a fast-paced world, meeting it with cutting edge of technolog ies and continuous advancements. ZEISS believes that innovation and technology are the key to a sustainable future and solutions for global change. We have a diverse range of portfolios throughout the ZEISS family in segments like, Industrial Quality & Research, Medical Technology, Consumer Markets and S emiconductor Manufacturing Technology . We are a global company with over 42,000 employees and have over 4,000 in the US and Canada alone! Make a difference, c ome join the team! Location/Region: This position is located in Dublin, CA. What 's the role? As a Staff Clinical Research Scientist , you get to work with an astonishing team that plays a vital role at Carl Zeiss Meditec, Inc. . Show case your skills and experience with process enhancement ( Sound Interesting? Here's what you'll do : The Staff Clinical Research Scientist is responsible for the day-to-day management of academics under contract as well as in-house Professional Affairs staff involved in applications development. Responsible for the management of clinical research teams in practices and university settings. With the VP of Professional Affairs, interacts with ophthalmology thought leaders worldwide Manage staff in the design and execution of clinical studies for the purpose of assessing the performance of current products, of applications under development or modification, and of competitors' products. Oversee the production of analyses and reports documenting clinical studies. Manage clinical research teams in the development and evaluation of new applications for new and existing products. Supervise evaluation of application performance and the Alpha testing of new applications and products. Primary contact for R&D and Marketing departments for internal application development projects and primary contact for external clinical sites. Maintain operational competence with most Carl Zeiss Meditec product Maintain computer and statistical skills consistent with needs of position. Maintain knowledge of corporate guidelines for Good Clinical Research Practices and of IRB procedures. Do you qualify? Four-year degree or equivalent with emphasis in the Physical Sciences, Mathematics, Statistics, or Engineering. At least seven (7) years experience in clinical research and in handling subjects and patients in a clinical research setting. Ability to move smoothly and professionally in the medical environment. The annual pay range for this position is $137,300 - $171,600. The pay offered for this role may be influenced by factors such as job location, scope of role, qualifications, education, experience, & complexity/specialization/scarcity of talent. This position is eligible for a Performance Bonus. ZEISS also offers robust benefits, including medical plans, retirement savings plan and paid time off. ZEISS is an EEO/AA/M/F/Disabled Veteran Employer Your ZEISS Recruiting Team: Jo Anne Mittelman Zeiss provides Equal Employment Opportunity without unlawful regard to an Applicants race, color, religion, creed, sex, gender, marital status, age, national origin or ancestry, physical or mental disability, medical condition, military or veteran status, citizen status, sexual orientation, pregnancy (includes childbirth, breastfeeding or related medical condition), genetic predisposition, carrier status, gender expression or identity, including transgender identity, or any other class or characteristic protected by federal, state, or local law of the employee (or the people with whom the employee associates, including relatives and friends).

Job Description:The Clinical Research Coordinator functions as a key component of the institution's research program assuring compliance with protocol requirements and quality control. Responsibilities include support of clinical trial services, preparation of IRC submissions, and recruitment of research subjects, coordinate care of research patients, and assist with protocol development and funding for identified research. The Clinical Research Coordinator assures compliance with Federal and State regulations relating to research and the study protocol requirements. Education: Bachelor's Degree Life Sciences - Required Experience: 2 years Research - Clinical Research - Required and 1 year Research Coordinator - Preferred Certifications/Licensures: BLS Basic Life Support - American Heart Association - Required CCRC Certified Clinical Research Coordinator - ACRP Association of Clinical Research Professionals - Preferred CPT1 Certified Phlebotomy Tech I - California Department of Public Health - Laboratory Field Services or CPT2 Certified Phlebotomy Tech II - California Department of Public Health - Laboratory Field Services Preferred On-site position only, remote work not available Work Shift:08.0 - 08:00 - 16:30 No Waive (United States of America) Pay Range: $48.85 - $73.28HourlyOffer amounts are based on demonstrated/relevant experience and/or licensure.Pay will be adjusted to the local market if hired outside of the Bay Area. Note: Positions at JMH which are exempt (not eligible for overtime) under the level of Manager are listed as hourly for compensation purposes on this posting. The work shift will contain the word ‘exempt' on it.Scheduled Weekly Hours:40

We are so glad you are interested in joining Sutter Health! **Organization:** SMCS-Valley Administration Coordinates and participates in clinical research studies. Gains confidence and cooperation from the patient, their family/support group, and other healthcare providers through competent job performance and effective communication. Adheres to all local/state/federal regulations, codes, policies and procedures to ensure privacy and safety while delivering optimal patient care. Strong interest in pediatrics and/or endocrinology disorders is preferred. **Job Description** : **EDUCATION:** **_Equivalent experience will be accepted in lieu of the required degree or diploma._** **Bachelor's: Science or Health - Related field** **CERTIFICATION & LICENSURE:** **BLS - Basic Life Support (must obtain it within 90 days)** **TYPICAL EXPERIENCE:** **1 + years of Clinical Trials Research** **_- preferred_** ** ** **SKILLS AND KNOWLEDGE:** **Knowledge of Federal and State regulations and International Guidelines related to Good Clinical Practices in clinical research.** **Ability to interpret a variety of data and instructions, furnished in written, oral, diagram, or schedule form.** **Possess written and verbal communications skills to communicate with fellow team members, supervisors, patients, and other hospital personnel.** **Well-developed time management and organizational skills, including the ability to prioritize assignments and work within standardized policies and procedures to achieve objectives and meet deadlines.** **General knowledge of computer applications, such as Microsoft Office Suite (Word, Excel, Access, and PowerPoint).** **Prioritize assignments and work within standardized policies and procedures to achieve objectives and meet deadlines.** **Work independently, as well as be part of the team, including accomplishing multiple tasks in an environment with interruptions.** **Identify, evaluate and resolve standard problems by selecting appropriate solutions from established options.** **Build collaborates relationships with peers and other staff members to achieve departmental and corporate objectives.** **Job Shift:** Days **Schedule:** Full Time **Shift Hours:** 8 **Days of the Week:** Monday - Friday **Weekend Requirements:** Occasionally **Benefits:** Yes **Unions:** No **Position Status:** Non-Exempt **Weekly Hours:** 40 **Employee Status:** Regular Employees of Sutter Health and its entities may handle hazardous drugs in the course of their work, including patient care, which requires them to manage, store, prepare, receive, unpack, transport, dispose of, or administer drugs identified as hazardous or potentially hazardous by the National Institute for Occupational Safety and Health (NIOSH) and in accordance with the USP 800 guidelines. Sutter Health is an equal opportunity employer EOE/M/F/Disability/Veterans. Pay Range is $33.26 to $49.89 / hour _The salary range for this role may vary above or below the posted range as determined by location. This range has not been adjusted for any specific geographic differential applicable by area where the position may be filled. Compensation takes into account several factors including but not limited to a candidate's experience, education, skills, licensure and certifications, department equity, training and organizational needs. Base pay is just one piece of the total rewards program offered by Sutter Health. Eligible roles also qualify for a comprehensive benefits package._

The Clinical Research Coordinator functions as a key component of the institution's research program assuring compliance with protocol requirements and quality control. Responsibilities include support of clinical trial services, preparation of IRC submissions, and recruitment of research subjects, coordinate care of research patients, and assist with protocol development and funding for identified research. The Clinical Research Coordinator assures compliance with Federal and State regulations relating to research and the study protocol requirements. Education: * Bachelor's Degree Life Sciences - Required Experience: * 2 years Research - Clinical Research - Required and * 1 year Research Coordinator - Preferred Certifications/Licensures: * BLS Basic Life Support - American Heart Association - Required * CCRC Certified Clinical Research Coordinator - ACRP Association of Clinical Research Professionals - Preferred * CPT1 Certified Phlebotomy Tech I - California Department of Public Health - Laboratory Field Services or * CPT2 Certified Phlebotomy Tech II - California Department of Public Health - Laboratory Field Services Preferred * On-site position only, remote work not available Work Shift: 08.0 - 08:00 - 16:30 No Waive (United States of America) Pay Range: $48.85 - $73.28 Hourly Offer amounts are based on demonstrated/relevant experience and/or licensure. Pay will be adjusted to the local market if hired outside of the Bay Area. Note: Positions at JMH which are exempt (not eligible for overtime) under the level of Manager are listed as hourly for compensation purposes on this posting. The work shift will contain the word 'exempt' on it. Scheduled Weekly Hours: 40

Role :Senior Reimbursement Coordinator Duration:C2H The Senior Reimbursement Coordinator acts as a liaison for Revenulytics, Customers and Payers. The Senior Reimbursement Coordinator will maintain high customer service standards, achieving overall customer satisfaction in providing timely and accurate information and service to all the clients. Primary Duties & Responsibilities • Act as a bridge between Avellino and their clients; they ensure client satisfaction by duly fulfilling requests. • Interact with clients and build relationships with them while ensuring their needs are being met • Oversee a team of third-party reimbursement coordinators and ensure they are providing an exceptional client experience (invoicing and follow up) • Mastermind creative ways to deliver an exceptional client experience • Resolve complex client billing problems or disputes in a professional manner • Coach and support revenue cycle team members to help them meet departmental goals • Keep records and documentation of client interactions for training purposes • They take responsibility of arising client issues and proffer recommendations useful in addressing such problems. • They coordinate and organize billing and collection projects as well as implement strategies necessary for attaining project goals. • They also monitor and ensure the customer relationship management database is up-to-date. Professional Experience & Qualifications • Bachelor's Degree in Business, Healthcare Administration, or related field as outline in the essential duties; or High School Diploma/General Education Degree and 4 years of relevant experience as outlined in the essential duties in lieu of Bachelor's Degree. • 5+ years of billing experience in public or private third-party reimbursement arena, practice management, or diagnostic/pharmaceutical industry . • Strong understanding of the Health Insurance Portability and Accountability Act of 1996 (HIPPA) and importance of patient data privacy. • Strong understanding of medical billing, explanation of benefits (EOB), payor policies, contracting changes and, coverage updates. • Demonstrated strong oral and written customer service skills and ability to think on your own feet • Proficient in Microsoft Office programs to include Word, Excel, Outlook, and Teams • Preferred: experience with laboratory work Aroha Technologies Inc.

As one of the nation's largest nonprofit systems, CommonSpirit Health now has more than 2,200 care sites and 140 hospitals in 24 states. We serve some of the most diverse communities across the nation, and in each location, humankindness leads the way. The CommonSpirit Health Research Institute offers comprehensive clinical research services and support for various research activities. Their primary focus includes multi-site clinical trials, local and large-scale data research, partnerships with industry and academia for technology and innovation research, physician-initiated research, resident-initiated research in teaching facilities, nurse-initiated research, and health sciences student-initiated research. The institute aims to provide start-to-finish research services and assist in advancing medical knowledge and patient care. CommonSpirit Health was formed by the alignment of Catholic Health Initiatives (CHI) and Dignity Health. With more than 700 care sites across the U.S. from clinics and hospitals to home-based care and virtual care services CommonSpirit is accessible to nearly one out of every four U.S. residents. Our world needs compassion like never before. Our communities need caring and our families need protection. With our combined resources CommonSpirit is committed to building healthy communities advocating for those who are poor and vulnerable and innovating how and where healing can happen both inside our hospitals and out in the community. **Responsibilities** The Clinical Research Associate (CRA) works with the CommonSpirit Health Research Institute Market Clinical Research Manager (MCRM) to support the planning, implementation and coordination of clinical trials and other research projects managed by the CommonSpirit Health Research Institute. Duties may vary depending on the size and complexity to each study. Under the direction of the MCRM and/or Senior Clinical Research Coordinator, the incumbent assists with clinical trial or other research project coordination duties as assigned, including but not limited to: research participant recruitment, screening and enrollment; completion of protocol required visits and procedures; collection and reporting of data; coordination of and participation in sponsor monitoring visits or federal audits; query resolution; adverse event reporting, source documentation and research record development and maintenance; study drug accountability; specimen collection, processing and shipment. Under the direction of the MCRM and/or Senior Clinical Research Coordinator, the incumbent helps to ensure compliance of the research program and its studies with all applicable federal and state regulations, as well as CommonSpirit Health policy. + Coordinate and participate in site initiation and other sponsor-required training for all protocols. + Dispense study medication to research participants under the direction of the PI, and/or coordinate study drug administration with hospital/clinic Pharmacy staff. + Process labs for clinical trials, including collecting, centrifuging and aliquoting specimens, and ship specimens in accordance with federal biologics shipping regulations. + Conduct informed consent process with research participants; document informed consent discussion and obtain signatures per protocol, federal, state and institutional requirements. + Coordinate all study-required visits, procedures, tests and activities to meet protocol requirements; schedule participant appointments with appropriate provider/facility. + Perform timely and accurate collection and reporting of data in accordance with protocol and sponsor requirements, applicable laws, and institutional policies. + Create source documentation forms/templates to ensure accurate collection of all study data; maintain research subject charts/binders to meet protocol requirements. + With appropriate training/credentialing, may perform blood draws, ECGs, and other testing, i.e., NIH Stroke Scale, as required by research protocols. + Identify and report all unanticipated and other adverse/serious adverse events, as well as protocol deviations, violations or exceptions, to the study sponsor and IRB as required by GCP, FDA, OHRP and CommonSpirit Health policy. + Prepare, manage and submit all required any required study/regulatory, documents, applications and forms, including but not limited to the applicable Institutional Review Board (IRB) application form(s), informed consent documents, 1572 forms, Conflict of Interest forms, and other forms as required by the sponsor, IRB, or CommonSpirit Health. + To ensure protocol adherence, accurate data collection and billing compliance, instruct/advise Principal Investigator (PI) and other health care providers in the hospital/ clinic setting as to protocol-required tests and procedures to be conducted at each visit. + Determine effective strategies for promoting/recruiting research participants and retaining participants in long term clinical trials. Actively recruit, screen and enroll participants in trials. + Attend investigator/coordinator meetings as required by study sponsors. + Serve as liaison between participants, physician investigators, sponsors of research, IRBs, CSHRI administration, patient care coordinators and insurance companies to assist in protocol interpretation, clinical and safety questions, and pre-authorization questions. + Prepare for, coordinate and participate in sponsor monitoring visits or internal/external audits; resolve queries and other findings promptly; prepare responses or corrective actions plans as needed. \#LI-CSH **Qualifications** + Minimum 3 years of experience conducting clinical trials required; worked as primary research coordinator for at least 5 drug or device trials. + Minimum 3 years of experience interacting with patients in a healthcare setting required. + Current certification (CCRP or CCRC) by the Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals (ACRP) required. + Current certificate of Human Subjects Protection and Good Clinical Practice training required. + Bachelor's degree in a science or health-related field or a combination of education and/or additional job-related experience in lieu of the degree, required. + Thorough knowledge and understanding of research regulatory requirements involving human subjects research, including FDA, OHRP and GCP requirements required. + Experience in implementation of research protocols and clinical trials processes required. + Experience in preparing and maintaining regulatory documents and other IRB-related study documentation required. + Experience using electronic data capture software required; Clinical Trial Management Systems (CTMS) preferred. + Lab processing experience required, Phlebotomy certification preferred. **Pay Range** $34.50 - $42.28 /hour We are an equal opportunity/affirmative action employer.

We are seeking a dedicated and enthusiastic Clinical Research Coordinator to join our team. This role is focused on patient-facing activities, including screening, recruitment, managing source documentation, and documenting in EMR. The coordinator will not be responsible for data entry or specimen collection, but will manage patient interactions and protocol compliance for oncology trials. Responsibilities * Screen, consent, and enroll patients in oncology trials, following patients through the course of their therapy. * Spend most of the time in clinic, seeing patients with doctors, attending patient visits, ensuring completion of questionnaires, and conducting research procedures. * Work with clinic staff to schedule appointments, such as EKGs and vitals. * Ensure protocol compliance by adhering to correct timeframes. * Interact and collaborate with nursing staff, medical assistants, and clinical staff for insurance authorizations and scheduling. * Work closely with infusion nurses to schedule patient appointments. * Support patients by providing them with specific calendars and checklists for their participation in the study, and help them manage side effects. Essential Skills * Clinical research experience * Proficiency in pre-screening patients, chart review, and patient recruitment. * Experience in oncology clinical studies (preferred), including screening, consenting, and source documentation. * Strong organizational skills and the ability to read protocols and notice side effects. * Bachelor's degree. Additional Skills & Qualifications * Experience with patient study enrollment and assisting patients with study requirements. * Ability to provide support for oncology patients, considering their serious health conditions. Pay and Benefits The pay range for this position is $30.00 - $40.00 Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Sacramento,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.

Location: Sacramento, California, United States of America Job ID: R-88488 undefined: Full Time undefined: Days undefined: Onsite undefined: 40 **Description** We are so glad you are interested in joining Sutter Health! **Organization:** Coordinates and participates in clinical research studies. Gains confidence and cooperation from the patient, their family/support group, and other healthcare providers through competent job performance and effective communication. Adheres to all local/state/federal regulations, codes, policies and procedures to ensure privacy and safety while delivering optimal patient care. Strong interest in pediatrics and/or endocrinology disorders is preferred.**Job Description**: ****EDUCATION:***Equivalent experience will be accepted in lieu of the required degree or diploma.*** * **Bachelor's: Science or Health - Related field** ****CERTIFICATION & LICENSURE:**** * **BLS - Basic Life Support (must obtain it within 90 days)** ****TYPICAL EXPERIENCE:**** * **1 + years of Clinical Trials Research *- preferred*** ** **SKILLS AND KNOWLEDGE:**** * **Knowledge of Federal and State regulations and International Guidelines related to Good Clinical Practices in clinical research.** * **Ability to interpret a variety of data and instructions, furnished in written, oral, diagram, or schedule form.** * **Possess written and verbal communications skills to communicate with fellow team members, supervisors, patients, and other hospital personnel.** * **Well-developed time management and organizational skills, including the ability to prioritize assignments and work within standardized policies and procedures to achieve objectives and meet deadlines.** * **General knowledge of computer applications, such as Microsoft Office Suite (Word, Excel, Access, and PowerPoint).** * **Prioritize assignments and work within standardized policies and procedures to achieve objectives and meet deadlines.** * **Work independently, as well as be part of the team, including accomplishing multiple tasks in an environment with interruptions.** * **Identify, evaluate and resolve standard problems by selecting appropriate solutions from established options.** * **Build collaborates relationships with peers and other staff members to achieve departmental and corporate objectives.** **Job Shift:** Days**Schedule:** Full Time**Shift Hours:** 8**Days of the Week:** Monday - Friday**Weekend Requirements:** Occasionally**Benefits:** Yes**Unions:** No**Position Status:** Non-Exempt**Weekly Hours:** 40**Employee Status:** RegularEmployees of Sutter Health and its entities may handle hazardous drugs in the course of their work, including patient care, which requires them to manage, store, prepare, receive, unpack, transport, dispose of, or administer drugs identified as hazardous or potentially hazardous by the National Institute for Occupational Safety and Health (NIOSH) and in accordance with the USP 800 guidelines. Sutter Health is an equal opportunity employer EOE/M/F/Disability/Veterans. Pay Range is $33.26 to $49.89 / hour*The salary range for this role may vary above or below the posted range as determined by location. This range has not been adjusted for any specific geographic differential applicable by area where the position may be filled. Compensation takes into account several factors including but not limited to a candidate's experience, education, skills, licensure and certifications, department equity, training and organizational needs. Base pay is just one piece of the total rewards program offered by Sutter Health. Eligible roles also qualify for a comprehensive benefits package.* Collects data used for multiple purposes, which may include process improvement activities and clinical effectiveness/research studies. Ability to prioritize assignments and work within standardized p... Location : San Francisco, California, United States of America Job ID : R-82856 Collects data used for multiple purposes, which may include process improvement activities and clinical effectiveness/research studies. 2 years experience conducting clinical research. Well-developed... Location : San Francisco, California, United States of America Job ID : R-80429 Location : Walnut Creek, California, United States of America

What We Do Care Access is delivering the future of medicine today! Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that limit participation among physicians and patients to 3%. By removing this bottleneck, Care Access is helping accelerate the approval and delivery of critical and life-saving therapies. Who We Are We care. Our people are the engines behind our mission: to revolutionize access to clinical trials for the benefit of patients everywhere. We care for one another, find new ideas to accelerate medicine, and seed a long-term impact for generations. Position Overview The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance. What You'll Be Working On Duties include but not limited to: ● Ability to understand and follow institutional SOPs. ● Review and assess protocol (including amendments) for clarity, logistical feasibility ● Ensure that all training and study requirements are met prior to trial conduct. ● Discuss study medication, required procedures, eligibility criteria and impact on office flow with Investigator and site staff. ● Assist with planning and creation of appropriate recruitment materials. ● Assist in development of recruitment plan and obtain listing of potential candidates to contact from subject database. ● Actively work with recruitment team in calling and recruiting subjects ● Attend Investigator meetings as required. ● Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with clinical staff and Sponsor/CRO representatives. ● Assist in the creation and review of source documents. ● Ensure adequate supplies have arrived on site for protocol initiation (lab kits, study medication, specialized equipment, IVRS/EDC access and passwords) Study Management: ● Prioritize activities with specific regard to protocol timelines ● Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials. ● Maintain effective relationships with study participants and other care Access Research personnel. ● Interact in a positive, professional manner with patients, sponsor representatives, investigators and Care Access Research personnel and management. ● Communicate clearly verbally and in writing. Patient Coordination: ● Prescreen study candidates ● Obtain informed consent per Care Access Research SOP . ● Complete visit procedures in accordance with protocol. ● Train others and complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc. ● Review laboratory results, ECGs, and other test results (e.g., MRIs) for completeness and alert values, ensuring investigator review in a timely fashion. ● Identify adverse events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor (where appropriate) Documentation: ● Record data legibly and enter in real time on paper or e-source documents ● Accurately record study medication inventory, medication dispensation, and patient compliance. ● Resolve data management queries and correct source data within sponsor provided timelines ● Assist regulatory personnel with completion and filing of regulatory documents. Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive. Physical and Travel Requirements · This is an on-site position with regional commute requirements. Regularly planned travel within the region will be required as part of the role. What You Bring Knowledge, Skills, and Abilities: ● Excellent working knowledge of medical and research terminology ● Excellent working knowledge of federal regulations, good clinical practices (GCP) ● Ability to communicate and work effectively with a diverse team of professionals. ● Strong organizational, prioritization and leadership skills and capabilities with a strong attention to detail ● Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel. ● Critical thinker and problem solver ● Friendly, outgoing personality; maintain a positive attitude under pressure. ● High level of self-motivation and energy ● Excellent professional writing and communication skills ● Ability to work independently in a fast-paced environment with minimal supervision. Certifications/Licenses, Education, and Experience: ● Bachelor's Degree preferred, or equivalent combination of education, training and experience. ● A minimum of 3 years prior Clinical Research Coordinator experience required ● Prefer 1 year of experience as a Care Access Research Clinical Research Coordinator ● Recent phlebotomy experience required Benefits (US Full-Time Employees Only) ● PTO/vacation days, sick days, holidays. ● 100% paid medical, dental, and vision Insurance. 75% for dependents. ● HSA plan ● Short-term disability, long-term disability, and life Insurance. ● Culture of growth and equality ● 401k retirement plan Diversity & Inclusion We serve patients and researchers from diverse cultures and communities around the world. We are stronger and better when we build a team representing the people we aim to support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. We value diversity and believe that unique contributions drive our success. At Care Access, every day, we are advancing medical breakthroughs. We're uniting standard patient care with cutting-edge treatments and research. Our work brings life-changing therapies to those in need and paves the way for newer and greater treatments to reach the world. We're proud to advance these breakthroughs and work with the big players while engaging with the physicians and caring for patients. We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. Care Access is currently unable to sponsor work visas. Employment Statement Care Access complies with all employment laws and regulations with respect to its employment practices, terms and conditions of employment, and pay equity and wages. Care Access does not engage in any unfair or forced labor practice and does not tolerate, under any circumstances, the use of any form of forced or involuntary labor, child labor, or human trafficking. This extends to suppliers, partners, or other third parties with whom Care Access does business. Care Access values and promotes the protection of human rights everywhere.

Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials. Science 37's extraordinary work environment allows continuous collaboration between clinicians, clinical researchers, patient recruitment specialists, data managers and technology developers. The Nursing Solutions Group is involved throughout the trial life cycle, from protocol development and feasibility analysis to clinical trial implementation and closeout. The Per Diem Mobile Research Nurse is a Registered Nurse who will work per diem and has experience across multiple therapeutic areas with the ability to work independently and integrate well with the Nursing Solutions Group. With interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. The Mobile Research Nurse ensures the professional delivery of patient care in compliance with all federal and state regulations, Good Clinical Practice, and Standard Operating Procedures. * This is a travel role that requires on-site visits to participants homes. Duties for this position include but are not limited to: * Participate and provide research nurse services to qualified study participants at home * Apply clinical research and nursing practices to develop solutions to complex problems * Collaborate with Lead and Per Diem Mobile Research Nurses on solutioning, education, and resource support * Participate in activities that will further the operational development of Science 37 nursing service delivery * Develop relationships with study team members and serve as the subject matter expert (SME) on all nursing processes * Other duties as assigned as the needs of Science 37 evolve and change This position has the following qualifications: * BSN degree preferred * Full Vaccination Required subject to applicable law: All Science 37 personnel who interact in person with trial participants must be fully vaccinated against COVID-19."Fully vaccinated" means having received both doses of the Pfizer or Moderna vaccines or the single-dose Johnson & Johnson vaccine. * Active RN licensure in home state as well as eligibility for Compact Licensure required * Minimum 2+ years clinical/research experience preferred * Basic Life Support (BLS) Certification * Maintain a positive reflection of the company by representation in participant's homes or in clinic settings * Travel and availability qualifications are as follows: * 1-2 days minimum a week dedicated to support Science 37's study visits * Weekday/night availability required * Must be willing to travel to a participants homes * Active Driver's License Science 37 is looking for people with the following skills and competencies: * BSN degree preferred * Active RN licensure in home state as well as eligibility for Compact Licensure required * Minimum 2+ years clinical/research experience preferred * Basic Life Support (BLS) Certification * Active Driver's License * Weekday/night availability required * Maintain a positive reflection of the company by representation in participant's homes or in clinic settings * Up to 100% travel, as needed, for study participant visits, project team meetings, and other professional meetings/conferences as needed * Ability to obtain nursing license in multiple states based on study needs * Physical ability to perform nursing tasks and lift equipment up to 15 kg in weight * Access to a reliable vehicle to perform study participant visits and transport equipment * Ability to drive to local and/or remote locations to perform study participant visits * Ability to use technology effectively and appropriately for study participant assessments and documentation including but not limited to study participant care equipment, laptop computers, communication devices and tablets * Ability to communicate in English (both verbal and written) There is minimal supervision for this position, with individuals reporting to the Manager, Nursing Solutions Group. Compensation varies based on location and work being performed. The starting pay range for a candidate selected for this position is generally within the range of $50-55 per hour. Employees may be eligible for additional discretionary bonuses and commissions. The successful candidate's actual pay will also be based on qualifications and experience, so the actual starting pay may be above or below this range. Science 37 is an equal opportunity employer. We are committed to creating a diverse environment and is an equal opportunity employer. All qualified applicants receive consideration for employment without regard to age, race, ethnicity (including but not limited to hair texture and protected hairstyles), ancestry, color, sex, national origin, sexual orientation, gender, gender identity, gender expression, transgender status, religious creed, physical or mental disability (including actual or perceived disability), medical condition (including HIV/AIDS), pregnancy, perceived pregnancy and pregnancy related conditions, genetic information, marital status, political affiliation or activities, status as a victim of domestic violence, assault, or stalking, veteran status or participation in the uniformed military services of the United States, including the National Guard, or any other basis prohibited by applicable law. Science 37 values the well-being of its employees and aims to provide team members with everything they need to succeed. Submit your resume to apply!