Clinical Research Coordinator: Trial Operations & Compliance

Tandem Intermediate LLC

Melbourne (FL)

On-site

USD 52,000 - 75,000

Full time

14 days+

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Job summary

Tandem Intermediate LLC is seeking a Clinical Research Coordinator (CRC) to oversee daily operational activities for assigned studies. You will coordinate study start-up, conduct consent discussions, manage data entry in EDC, and maintain regulatory files.

Responsibilities include coordinating visits, safety reporting, and sponsor/CRO communications while ensuring adherence to SOPs and GCP standards. Bachelor's degree and 2 years in clinical research are required.

Qualifications

Bachelor's degree in a related field is required.
Minimum of two (2) years of clinical research or trial management experience.
Phlebotomy experience is required.
Preferred credentials include MS, LPN, or RN licensure.
Proficiency with regulatory compliance and study documentation.

Responsibilities

Coordinate all aspects of assigned clinical trials from initiation through close-out.
Support study start-up activities including feasibility, regulatory submissions, and site activation.
Attend investigator meetings, site initiation visits, and other study-related meetings.
Manage visit schedules and coordinate study-related activities across clinical teams.
Conduct informed consent discussions with participants and document consent.
Monitor and report adverse events to the PI, sponsor, and IRB as required.
Maintain source documentation, CRFs, regulatory files, and study records.
Enter study data into EDC and other required systems; resolve sponsor or monitor queries.