Clinical Trial Internship (4-6months)

Location: Petaling Jaya, Selangor

Job Descriptions:

• Trial and Site Administration
  • Track key study documents and safety reports.
  • Distribute and manage study materials and documents.
  • Update clinical trial systems (CTMS) and trackers.
• Document Management
  • Prepare and handle study documents and correspondence.
  • Distribute, ship, and archive clinical documents (e.g. eTMF).
  • Assist with document reconciliation and maintain Investigator Site Files.
• Meeting Support
  • Organize study-related meetings and prepare related documents.
  • Support investigator meetings (invitations, materials, venue, and coordination).
• Local Support
  • Create simple communication materials such as posters and videos.
  • Support process improvements using digital tools (e.g. automation, coding, AI).
  • Support site management activities under the guidance of Sr. CRA/CRA, including site start-up, maintenance, and close-out to ensure sites are inspection-ready.

• The intern will receive online and on-the-job training to understand the roles of Clinical Research Associate and Clinical Trial Coordinator.

Job Requirements:

• Bachelor in Pharmaceutical, Healthcare, Biomedical, or relevant studies.
• Effective communication and problem-solving skills.
• Good organization and time management skills.
• Able to work independently and collaborate effectively with others.
• Adaptable and flexible.
• Administrative and documentation skills.
• Able to do a 6-month internship, preferably.
• Able to start the internship somewhere in Mid/End-June or Early July

What you will experience in this role:

• Learn various systems such as CTMS, eTMF, and others.
• Experience Phase 1 to Phase 4 process of the clinical trial.
• Documentation and regulatory compliance.

Others Information:

For those who have what it takes, please send in resume to:

Consultant in Charge: Wei Li

Email: weili@brightprospect.com.my