Independently coordinate low- to moderate-complexity trials, including scheduling, visit execution, and day-to-day operations.

Serve as secondary CRC on high-enrolling screening trials, supporting screening, enrollment, and participant follow-up.

Conduct participant visits per protocol, including medical/psychiatric history collection, vitals, ECGs, phlebotomy, and specimen processing, as trained.

Prepare and maintain study source documents, lab kits, CRFs, and visit materials.

Ensure accurate, ALCOA+-compliant documentation of all study procedures and maintain required logs, trackers, and regulatory files.

Support investigational product (IP) accountability for assigned studies, including receipt, storage, dispensing, reconciliation, temperature monitoring, and documentation under supervision, ensuring compliance with protocol and site SOPs.

Communicate with participants between visits to maintain engagement and protocol compliance.

Assist with sponsor communication, monitoring visit preparation, and audit readiness as appropriate.

Contribute to query resolution, data cleaning, and study metrics tracking to support accurate reporting and inspection readiness.

Support screening operations and meet enrollment expectations for assigned study tasks.

Prepare internal reports or summaries for review under guidance from CRC II/III.

Clinical Research Coordinator I

Responsibilities

Qualification

Required

Benefits

Company

Adamsclinical

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