Clinical Trials Coordinator: Study Ops, Data & Compliance
Listed on 2026-10-07
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Healthcare
Clinical Research
Tandem Intermediate LLC is seeking a Clinical Research Coordinator to oversee daily operations of assigned clinical trials. You will work with investigators, sponsors, and CROs to ensure studies comply with protocols, regulatory requirements, and ethical standards.
Key duties include study start-up, participant recruitment, informed consent, data entry in EDC, and sponsor communications, while maintaining source documentation and trial records in good order.
We are seeking a motivated Clinical Trials Coordinator:
Study Ops, Data & Compliance to join Tandem Intermediate LLC in Marrero, LA, United States.
Step into the Clinical Trials Coordinator:
Study Ops, Data & Compliance role at Tandem Intermediate LLC in Marrero, LA, United States and grow with us.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
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