Sr. Clinical Research Coordinator (Onsite)
This is a 6+ month assignment
Assignment Overview:
Our client is an innovative biopharmaceutical company who is committed to delivering life-changing therapies for rare diseases. Our client needs a Clinical Research Coordinator to support one of their leading clinical sites with prospective and retrospective clinical research studies. This assignment offers clinical professionals an opportunity to work toward greatly improving patient’s lives.
Primary Responsibilities:
- Maintains research practices using Good Clinical Practice (GCP) guidelines
- Recruit and screen potential study participants
- Performs intake assessments/interviews
- Create and/or maintain all documents and records related to the study
- Responsible for ensuring that all procedures comply with regulatory procedures and standard operating procedures
- Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress.
- Manage the inventory of equipment and supplies related to the study as needed
- Collect data and patient information into electronic systems (EMR), for prospective and retrospective clinical studies.
- Create reports on each study, including notes on protocols, workload, data collection, etc.
- Work closely with Sponsor and assisting CRO.
Technical Requirements
- 7+ years of experience working in as a clinical research coordinator (pharmaceutical)
- Bachelor’s Degre - (RN preferred)
- Strong knowledge and understanding of principles of GCP and appropriate FDA regulations related to clinical research.
- Phlebotomy certification preferred
- Experience with rare diseases preferred
Job Type: Contract
Pay: From $35.00 per hour
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Schedule:
Ability to Commute:
Ability to Relocate:
- La Jolla, CA: Relocate before starting work (Required)
Work Location: In person