Clinical Research Coordinator

1. Manage administrative tasks related to the research project.
2. Ensure research processes strictly follow study protocols and maintain accurate data collection from all sources.
3. Recruit participants, provide comprehensive information about the project, and serve as the primary contact person for study participants.
4. Coordinate effectively with the study team, including doctors, lab analysts, pharmacists, nurses, and front office staff.
5. Prepare and submit regular reports on study activities to the CRS team.

Requirements:

• Bachelor’s degree in Medicine with active professional license.
• Demonstrated ability to communicate in written and spoken English; is preferred
• Good interpersonal and communication skills.
• Good understanding and knowledge of Good Clinical Practice (GCP) and experiences in clinical trials is preferred.
• Open to work in a team work & individual; to organize a team or a group of trials participants.
• Responsive, creative, and adaptable to manage changes and solving problems.
• Willing to be placed in Siloam Jakarta Area.

Our team will review your application and will be in touch if your application is shortlisted to the next stage.

We wish you the best. Have a great day!