Clinical Trials Coordinator: Recruitment, Data & Protocols

Siloam Hospitals Group; Jakarta Pusat; Sur place; IDR 60 000 000 - 100 000 000; Plein temps

Résumé du poste

Siloam Hospitals Group in Jakarta is seeking a Clinical Research Coordinator to support a research project. You will manage administrative tasks, ensure protocols are followed, and maintain accurate data collection.

You will recruit participants, provide information about the project, and serve as the main contact for study participants, while coordinating with doctors, nurses, lab staff, and front office. The role requires a medical or public health degree, good English communication, and the

Qualifications

• Bachelor’s degree in Medicine (dr.)/ Biomedicine/ Public Health/ other related major.
• 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.

Responsabilités

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

Connaissances

Communication

English proficiency

Interpersonal skills

Team coordination

Formation

Bachelor’s degree in Medicine/ Biomedicine/ Public Health

Description du poste

Siloam Hospitals Group in Jakarta is seeking a Clinical Research Coordinator to support a research project. You will manage administrative tasks, ensure protocols are followed, and maintain accurate data collection.

You will recruit participants, provide information about the project, and serve as the main contact for study participants, while coordinating with doctors, nurses, lab staff, and front office. The role requires a medical or public health degree, good English communication, and the