Clinical Research Coordinator C

Clinical Research Coordinator C

Job Description Summary

Job Description

Job Responsibilities

• Coordinate the conduct of Phase I – IV clinical trials.
• Participate in the conduct of audits by study sponsors, Clinical Research Organizations (CROs), the FDA, and other entities as required.
• Activate participation in the development of investigator-initiated protocol case report forms and progress notes
• Conduct initiation, monitoring and closeout visits with sponsors and/or CROs.
• Organize and maintain all documentation required by sponsor or CRO (source documentation, case report forms, study and regulatory binders, and patient binders).
• Resolve data queries with sponsor and CROs
• Recruit, screen and enroll potential study patients as specified per protocol.
• Process and ship blood, urine and serum specimens for each trial
• Schedule patient visits and any necessary testing