PT Biometrik Riset Indonesia is a leading Indonesian clinical research organization (CRO) specializing in Bioavailability & Bioequivalence (BA/BE) studies and clinical trials. We are committed to delivering ethical, high-quality and regulatory-compliant research in accordance with ICH-GCP, Indonesian GCP (CUKB) and BPOM regulations, supporting national and international pharmaceutical development.
Qualifications :
- Medical Doctor (GP or Specialist) with a valid and active STR.
- GCP Certification (preferred).
- Strong interest in Clinical Research and Clinical Trials.
- Good understanding of research ethics and subject safety.
- Detail-oriented and able to work in a multidisciplinary team.
Additional Experience (Advantageous) :
- Previous experience in clinical trials (any role).
- Familiarity with BPOM regulations and ethics committee processes.
- Exposure to BA/BE studies or clinical trials (Phase I–IV).
Key Responsibilities :
- Act as the responsible physician for BA/BE studies and Clinical Trials.
- Ensure compliance with ICH-GCP, CUKB, BPOM regulations, and study protocols.
- Conduct subject screening, medical evaluations, and clinical monitoring.
- Assess and manage Adverse Events (AE) and Serious Adverse Events (SAE).
- Coordinate with research teams, sponsors, CRO partners, and ethics committees.
- Review and sign medical records and study-related documentation.
Deadline for registration: February 13, 2026