Site Study Physician — Clinical Research Lead

Oxford University Clinical Research Unit; Papua; On-site; IDR 167,400,000 - 267,840,000; Full time

Job summary

The Oxford University Clinical Research Unit in Indonesia invites applications for a full-time position in Clinical Research Management and Governance. The role involves organizing clinical research activities at the site and supervising study teams, daily monitoring, and ensuring protocol compliance.

Key tasks include obtaining informed consent, conducting physical exams and ECGs, screening participants, managing visits, reporting SAE/AE as required, and coordinating communications with the

Qualifications

• Medical doctor with at least 1 year of clinical/research experience.
• BLS and ACLS certification required.
• Excellent written English and Bahasa Indonesia.
• Computer literacy and proficiency with standard software.
• Strong interpersonal and organizational skills.
• Ability to work in a team and manage complex research tasks.
• Experience in malaria research is advantageous.
• Willing to be located at the trial site for the contract period.

Responsibilities

• Organise clinical research activities at site and supervise study team daily.
• Carry out protocol tasks: informed consent, physical exams, vital signs, ECG, blood draws.
• Screen potential participants per protocol criteria.
• Manage participant visits and home/worship follow-ups as needed.
• Report SAE/AE to PI or safety personnel promptly and coordinate follow-up.
• Coordinate transport/evacuation for emergencies and SAE cases.
• Document protocol deviations timely and accurately.
• Ensure activities align with GCP, CUKB and local regulations.

Skills

Excellent English

Excellent Bahasa Indonesia

Computer literacy

Interpersonal skills

Organizational skills

Teamwork

Research experience

Attention to detail

Education

Medical Doctor

Tools

MS Office

Job description

The Oxford University Clinical Research Unit in Indonesia invites applications for a full-time position in Clinical Research Management and Governance. The role involves organizing clinical research activities at the site and supervising study teams, daily monitoring, and ensuring protocol compliance.

Key tasks include obtaining informed consent, conducting physical exams and ECGs, screening participants, managing visits, reporting SAE/AE as required, and coordinating communications with the