What are the responsibilities and job description for the Clinical Research Coordinator position at Apsida Life Science?
We Are currently Recruiting for a Clinical Research Coordinator (CRC) for our CRO Client based in Fort Collins, Colorado
Contract Terms:
- 60 days contract ( Immediate Start)
- 40 hours per week
- Potential to extend but not guaranteed.
Key Responsibilities
Study Coordination:
- Oversee the day-to-day operations of clinical trials.
- Recruit, screen, and enroll eligible participants.
- Schedule and coordinate study visits, procedures, and follow-ups.
Regulatory Compliance:
- Ensure studies adhere to Good Clinical Practice (GCP), Institutional Review Board (IRB) guidelines, and other regulatory standards.
- Prepare and submit regulatory documents to IRBs and other oversight bodies.
- Maintain study documentation and ensure proper record-keeping.
Data Management:
- Collect, record, and manage study data accurately.
- Ensure data integrity and confidentiality.
- Assist with data analysis and reporting as needed.
Participant Care:
- Serve as the primary point of contact for study participants.
- Educate participants about the study, including risks, benefits, and procedures.
- Monitor participant safety and report adverse events.
Team Collaboration:
- Work closely with principal investigators (PIs), sponsors, and other research staff.
- Facilitate communication between all parties involved in the study.
Budget and Resource Management:
- Assist with budgeting and financial management for studies.
- Manage study supplies and equipment.
