- Complete appropriate therapeutic, protocol and clinical research training to perform job duties and obtain knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines
- Under close supervision, administer protocol and related study training to assigned sites
- Assist in creation, maintenance and periodic review of Trial Master File, other clinical documentation, and project/study files to ensure quality, accuracy and completeness.
- Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow, and ensure proper archive of study-related documents such as site manuals, SUSAR, paper CRFs, DCFs and reference tools.

Clinical Research Associate (CRA) Intern
Internship @ClinChoice Clinical Research Sdn BhdJob Description
The Clinical Research Associate (CRA) Intern will participate in our in-house training program led by an instructor to gain knowledge and skills required to conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements as well as providing administrative support to our Clinical Operations teams to ensure timely and efficient execution of clinical trials. In addition, the individual will also gain exposure in study procedures by working with experienced clinical staff in Clinical Research Associate roles through on the job training and undertaking observational site monitoring visit.

