Clinical Research Coordinator (CRC)

Job Description

Assist investigators in the on-site execution of clinical trials, ensuring compliance with GCP regulations.

Requirements

• •Full-time bachelor’s degree or higher in Nursing, Pharmacy, Clinical Medicine, or related fields.
• •CET-4 or above preferred; excellent English reading and writing skills.
• •Proficient in Microsoft Office and other office software.
• •Strong communication skills, service orientation, and teamwork spirit; responsible, proactive, meticulous, detail-oriented, and well-organized.

Responsibilities

• 1 Assist in the collection, organization, and archival management of clinical trial project documentation.
• 2 Assist with subject screening and enrollment activities for clinical trials conducted in hospitals.
• 3 Assist in the collection, processing, storage, and transportation of trial specimens.
• 4 Assist in the management and accountability of investigational products (IP), including receipt, storage, dispensing, retrieval, return, and completion of related records.
• 5 Assist investigators in completing Case Report Forms (CRFs).
• 6 Assist investigators in tracking subject follow-up visits.
• 7 Assist investigators with other relevant tasks related to clinical trials.

Benefits