Unblinded Clinical Research Coordinator (CRC)

Job Description : Unblinded Clinical Research Coordinator

• need IP, investigational drug experience if no clinical research experience prior

The Unblinded Clinical Research Coordinator (CRC) is responsible for supporting the daily operations of assigned clinical trials and ensuring all study procedures are performed according to protocol, regulatory requirements, and site standard operating procedures (SOPs).

In this unblinded capacity, the CRC’s primary role is to manage the Investigational Product (IP) throughout the study lifecycle, including receipt, storage, dispensing, administration, return, and destruction. The Unblinded CRC also ensures that study blinding is maintained for trials requiring separation of blinded and unblinded staff roles and serves as the subject matter expert for IP handling and documentation.

Reports To :

Site Manager or Director

Core Responsibilities

Clinical Research Coordination

Unblinded Study Responsibilities

Investigational Product (IP) Management

Required Skills & Abilities

Education & Experience