Clinical Research Coordinator I
Cedars-Sinai
Posted 14 Nov 2026, 12:29 ET
This job at a glance
- Who can apply
- New grads and up to 1 year · Diploma
- Must know
- PhlebotomyOperationsRecruitingAuditingCPR / BLS
- Nice to have
- Patient care
- Work
- On-site in Los Angeles
- Pay
- Not stated by the employer.
- Skill demand
- Operations35%Recruiting30%Auditing18%Phlebotomy9%of 99 similar entry-level jobs posted in the US this week
- Listed
- Nov 14, 2026 · still open
Sign in free to see which of these skills your resume already shows.
About the Role
Cedars-Sinai's The Angeles Clinic & Research Institute is seeking a Clinical Research Coordinator I, Laboratory (Onsite) with Phlebotomy CPT I certification. This role supports clinical research protocols within the department, contributing to the development of new cancer therapies and patient care.
Key Responsibilities
- Process research laboratory specimens accurately, including centrifuging, aliquoting, storing, and shipping.
- Monitor sponsor deliveries, manage inventory of kits and supplies, and maintain electronic records.
- Perform administrative functions for research studies, including scheduling patients, maintaining consent forms, case report forms, SAEs, and source documents.
- Facilitate patient screening and recruitment, explain non-medical trial concepts, and support the informed consent process.
- Coordinate logistical aspects of clinical research projects, including planning and resource projection.
- Ensure accurate and timely data collection, documentation, entry, and reporting; respond to sponsor queries.
- Schedule and participate in monitoring and auditing activities, implementing corrective actions as needed.
- Compile and report on study information, including protocol activity, accrual data, and workload.
- Submit adverse events, serious adverse events, protocol deviations, and Safety Letters to the IRB in accordance with guidelines.
- Act as a liaison with pharmaceutical company representatives to monitor project progress.
- Provide assistance with research finance billing, distinguishing routine care from research-related care.
- Attend meetings and conferences related to research activities.
Requirements & Tech Stack
- High School Diploma or GED required.
- Associate degree or college coursework in a related field (e.g., Life Sciences, Health Sciences) preferred.
Qualifications
- Minimum of six (6) months of healthcare-related or clinical research experience required.
- Phlebotomy and/or laboratory assistant experience with demonstrated proficiency.
- One (1) year of experience as a Clinical Research Coordinator, Clinical Research Associate, or Clinical Research Assistant preferred.
- Current Certified Phlebotomy Technician I (CPT I) license issued by the State of California required.
- Current Basic Life Support (BLS) certification from the American Heart Association or American Red Cross required. (Certification must be valid for at least 60 days beyond anticipated start date).
- This role is 100% onsite.