Clinical Research Coord, I

MemorialCare; Fountain Valley (CA); On-site; USD 51,000 - 74,000; Full time

Benefits offered by this job

Health insurance

Bonus opportunities

Shift incentives

Job summary

MemorialCare Health System in Fountain Valley/Long Beach is seeking a Clinical Research Coordinator I to support recruitment, enrollment and follow-up in clinical trials across therapeutic areas. Under supervision, you will coordinate trial participation, ensure protocol compliance, and maintain regulatory documentation.

The role requires collaboration with study teams, adherence to GCP/ICH and FDA regulations, and participation in after-hours coverage if needed.

Responsibilities

• Enlist, maintain, and assure protocol compliance for all study participants.
• Collaborate with study investigators to determine eligibility and enroll participants.
• Screen potential participants for protocol eligibility and obtain informed consent.
• Ensure research quality by following SOPs, GCP, and applicable regulations.
• Coordinate patient care per protocol; may disburse investigational drug and educate participants on administration.

Job description

Title: Clinical Research Coordinator I

Location: Fountain Valley/Long Beach

Department: Research Admin

Status: Full Time

Shift: Days

Pay Range*: $37.27/hr - $54.01/hr

At MemorialCare Health System, we believe in providing extraordinary healthcare to our communities and an exceptional working environment for our employees. Memorial Care stands for excellence in Healthcare. Across our family of medical centers, we support each one of our bright, talented employees in reaching the highest levels of professional development, contribution, collaboration and accountability. Whatever your role and whatever expertise you bring, we are dedicated to helping you achieve your full potential in an environment of respect, innovation and teamwork.

Position Summary

The Clinical Research Coordinator fulfills the requirements of recruiting, enrolling and conducting follow-up of study participants in clinical trials related to all therapeutic areas represented throughout MemorialCare. In doing so, the Clinical Research Coordinator I is responsible for coordinating trial participation of study volunteers with the trial's protocol, company and trial Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/ International Conference on Harmonization (ICH) guidelines, FDA regulations and other applicable regulations (global, state, etc.). The Clinical Research Coordinator I is responsible for working with the trial delivery team to meet enrollment and retention goals and ensure compliance with the study protocol. After hours support and coverage may be needed to adequately meet the needs of the research subject and/or adhere to the protocol recruitments. After-hours Support Staff will be compensated for his/her time providing support during these after hours.

Essential Functions and Responsibilities of the Job

1. Under direct supervision of the Director of Clinical Operations, Manager of Clinical Operations and principal investigator, the CRC 1 is responsible for enlisting, maintaining, and assuring protocol compliance for all study participants in clinical trials.
2. Collaborates with study investigator in determining eligibility of potential participants in clinical trials.
3. Screens potential participants for protocol eligibility. Presents trial concepts and details to the participant, participates in the informed consent process, and enrolls participants in study protocol.
4. Ensures research quality by practicing in compliance with Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations.
5. Coordinates patient care in compliance with protocol requirements. May disburse investigational drug and provide participants' education regarding medication administration. Maintains investigational drug accountability, when needed, in cases where the Research Pharmacy is not maintaining that responsibility.
6. In collaboration with the study investigator, reviews study participants for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings.
7. Responsible for accurate and timely data collection, documentation, entry, and reporting. Schedules and participates in monitoring and auditing activities.
8. Maintains current and accurate documentation in the regulatory binder(s) as required by regulations and sponsors.
9. Participates in required training and education programs. Responsible for education of other personnel and vendors regarding clinical research.
10. Provide a safe environment for study participants, caregivers, and study personnel at all times through compliance with all federal, state, and professional regulatory standards. Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
11. Participates in the after-hours support and coverage schedule, if necessary.
12. Be at work and be on time.
13. Interact in a positive and constructive manner.
14. Follow company policies, procedures and directives.

*Placement in the pay range is based on multiple factors including, but not limited to, relevant years of experience and qualifications. In addition to base pay, there may be additional compensation available for this role, including but not limited to, shift differentials, extra shift incentives, and bonus opportunities. Health and wellness is our passion at MemorialCare-that includes taking good care of employees and their dependents. We offer high quality health insurance plan options, so you can select the best choice for your family. And there's more... Check out our MemorialCare Benefits for more information about our Benefits and Rewards.