What are the responsibilities and job description for the Senior Clinical Research Coordinator position at Syri Research?
About Us
Syri Research Center is a clinical research site dedicated to advancing medicine through high-quality Phase I–IV clinical trials. We partner with physicians, pharmaceutical sponsors, and patients to bring innovative therapies to the community.
Position OverviewWe are seeking an experienced Senior Clinical Research Coordinator (CRC) to manage clinical trials from start-up through close-out while ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP).
Responsibilities- Coordinate day-to-day clinical trial operations
- Screen, recruit, and enroll study participants
- Conduct informed consent and schedule study visits
- Maintain source documentation and regulatory binders
- Enter and manage data in EDC systems
- Ensure compliance with FDA, IRB, and GCP guidelines
- Prepare for sponsor monitoring visits and audits
- Report adverse events and protocol deviations
- Bachelor’s degree in health science, biology, nursing, or related field
- 2–5 years of clinical research experience
- Knowledge of FDA regulations, GCP, and clinical trial protocols
- Experience managing regulatory documents and study data
- Strong organizational and communication skills
- CRC certification (CCRC or equivalent)
- Experience with Phase I–IV trials
- Familiarity with EDC systems such as REDCap or Medidata
Submit your resume through LinkedIn.