Medical Monitor Job in Pretoria | Population Council | JobsNoti
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The Population Council is an international, non-profit, non-governmental organization. The Council conducts research in biomedicine, social science, and public health and helps build research capacities in developing countries. One-third of its research relates to HIV and AIDS; while its other major program areas are still linked to its early foundation in reproductive health and its relation to poverty, youth, and gender.
Job Information:
- Job Title: Medical Monitor
- Job Location: Fully Remote
- Country: South Africa
- Office: Population Council in Pretoria
- Assignment Length: 3 year fixed-term contract
- Application Deadline: 08 December 2025
Responsibilities:
To perform this job successfully, the individual must be able to perform each essential duty satisfactorily
Protocol and Funding Proposal Development
- Contribute to the development of funding proposals and initiate new proposals as needed.
- Respond to questions from Institutional Review Boards (IRBs) and National Regulatory Authorities (NRAs).
- Provide input into protocol development and study design.
Study Conduct and Clinical Oversight
- Lead the development and review of clinical Standard Operating Procedures (SOPs).
- Contribute to the development of Manuals of Procedures (MOPs) and Site-Specific Protocols (SSPs).
- Provide input on Case Report Forms (CRFs) to ensure accurate medical data collection.
- Train internal Population Council teams and research sites on clinical procedures, in coordination with the Senior Clinical Program Manager.
- Conduct ongoing medical review and monitoring of study conduct, including interpretation of laboratory findings and clinical data in collaboration with investigators.
- Participate in advisory committee meetings such as DMC, DSMB, and PSRT.
- Liaise with the Medical Safety team on adverse event (AE) assessments.
- Review all medically related protocol deviations and ensure appropriate corrective actions
CSR and Manuscript Development
- Provide input into statistical analysis plans.
- Review and provide input into Clinical Study Reports (CSRs).
- Initiate and contribute to scientific manuscripts related to study findings.
Additional Responsibilities
- Mentor and train team members.
- Provide input into new research funding proposals.
- Conduct medical monitoring for other assigned projects.
- Serve as backup Safety Physician and Deputy QPPV (South Africa).
- Collaborate closely with cross-functional teams to ensure alignment between clinical, safety, and operational activities.
Qualifications and Experience:
Education/Experience
- Medical degree (MD or equivalent) with registration with the appropriate medical council as a medical doctor.
- Minimum of 7–10 years’ experience in clinical research, medical monitoring, and project oversight.
- Experience in clinical trial design, conduct, and medical safety.
- Experience in HIV research or reproductive health research is an advantage.
- Knowledge of ICH-GCP guidelines, local regulations, and international clinical trial standards.
Knowledge, Skills, and Abilities
- Collaboration
- Communication Skills
- Problem-Solving
- Adaptability & Flexibility
- Attention to Detail
How to Apply:
Interested candidates should send their application through Online [Apply-Now]. For more details visit official website: popcouncil.org
