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The Psychiatric RN PRN oversees clinical study activities, ensuring ethical documentation and care for study participants while liaising with sponsors and maintaining communication and compliance with protocols.

The Pharmacist coordinates and supports clinical drug trials, oversees pharmacy operations, dispenses medications, trains staff, and ensures adherence to protocols and regulations.

Coordinate and support investigational drug trials by preparing and dispensing study medication, maintaining IP logs and storage, monitoring pharmacy procedures, attending sponsor/site meetings, ensuring protocol and regulatory compliance (FDA, ICH, GCP), and assisting with training and documentation.

The Data Entry Coordinator I transcribes clinical research data into electronic systems, maintains professional relationships, and ensures compliance with regulatory standards under moderate supervision.

Assist in coordinating clinical trials, ensuring adherence to regulations, organizing research information, and documenting study-related data.