Research medical officer / sub-investigator (Clinical Trials)
Company: CBTHR
- Location: Kwazulu/Natal, South Africa
- Work mode: On-site
- Employment type: Full-time
- Posted: Today
- Offer language: English
Job description
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
