Medical Monitor Job in Pretoria | Population Council | JobsNoti

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Jobs in South Africa
Jobs in South Africa

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