Research Medical Officer jobs

We are seeking a qualified and dynamic Medical Doctor (Sub-Investigator) to join our clinical research team on a fixed-term basis in Ilembe District, KZN. Under the direct supervision of the Principal Investigator (PI), the Sub-Investigator will do gynaecological investigations, manage day-to-day clinical trial activities, provide medical care to study participants, ensure strict adherence to trial protocols, and maintain compliance with ICH-GCP (International Conference on Harmonisation – Good Clinical Practice) guidelines and local regulatory standards.

Female Genital Schistosomiasis_ lesion recognition training/colposcopy _must start immediately and the candidate must pass a (refresher) exam in this before starting (organised by research team).

Key Responsibilities

• Lead and supervise site clinical and nursing teams.
• Oversee screening, recruitment, and enrollment of eligible study participants according to protocol inclusion/exclusion criteria.
• Conduct medical evaluations, review clinical histories, and monitor participant health status.

Safety & Compliance:

• Identify, manage, and promptly report Adverse Events (AEs) and Serious Adverse Events (SAEs) to the sponsor, ethics committees, and regulatory bodies.
• Ensure complete and accurate completion of Case Report Forms (CRFs), source documentation, and query resolutions.
• Assist and host clinical trial monitors during on-site monitoring visits.
• Study Operations & Collaboration:
• Coordinate with the Trial Management Group, pharmacy, and laboratory services.
• Contribute to study documentation, Standard Operating Procedures (SOPs),

Requirements & Qualifications

• Medical Degree (MBChB / MBBCh / MD) from a recognized institution.
• Active registration with the Health Professions Council of South Africa (HPCSA) as a Medical Practitioner.

Experience:

• Minimum of 2 years of clinical experience
• Prior hands-on experience in gynaecology, as a Sub-Investigator or Research Medical Officer in clinical trials preferred.

Certifications & Insurance:

• Valid SA Good Clinical Practice (GCP) training certificate.
• Ethics in Health Research Certificate
• Active HPCSA Malpractice Insurance policy (e.g., MPS).

Skills:

• Strong clinical decision-making, phlebotomy/cannulation skills, and patient care capabilities.
• Familiarity with data protection frameworks (POPIA) and research governance.

Payment per study participant

Job Types: Full-time, Temporary
Contract length: 4-7 months

License/Certification:

• HPCSA certificate minimum for for Medical Doctor (Required)

Work Location: In person