Independent Clinical Monitor

• Train Research Assistants and Principal Investigators on Good Clinical Practice (GCP) in line with FDA, Ghana Health Service, and CHAG requirements.
• Prepare clinical trial sites for GCP inspections and trial close-out activities.
• Support clinical trial site activation and provide training before the commencement of clinical trials.
• Monitor participant recruitment and identify potential risks that may affect study timelines, quality, or compliance.
• Conduct routine monitoring visits to ensure adherence to study protocols, regulatory requirements, and ethical standards.
• Prepare and submit comprehensive monitoring reports to the Food and Drugs Authority (FDA) Ghana.
• Advise the National Principal Investigator and Site Principal Investigators on GCP inspections and regulatory compliance.
• Identify protocol deviations and recommend appropriate corrective and preventive actions.
• Maintain accurate documentation of monitoring activities and findings.
• Perform any other duties assigned by the National Principal Investigator.

• Bachelor's degree in Medicine, Pharmacy, Nursing, Biomedical Sciences, Public Health, or a related health science field. A postgraduate qualification is an advantage.
• Certification or formal training in Good Clinical Practice (GCP).
• Minimum of 3–5 years of experience in clinical research monitoring, clinical trial management, or a related role.
• Experience working with regulatory bodies such as FDA Ghana, Ghana Health Service, or CHAG is an added advantage.

• Strong knowledge of ICH-GCP guidelines and clinical trial regulations.
• Excellent understanding of clinical research processes and regulatory compliance.
• Strong analytical, problem-solving, and risk assessment skills.
• Excellent report writing and documentation skills.
• Strong communication and interpersonal skills.
• Ability to work independently and manage multiple clinical sites.
• Willingness to travel to study sites as required.
• High level of integrity, professionalism, and attention to detail.
• Proficiency in Microsoft Office Suite.

• Competitive remuneration.
• Opportunity to contribute to impactful clinical research.
• Professional and collaborative work environment.
• Opportunities for continuous learning and professional development.

Location: University for Development Studies (UDS), Tamale, Northern Region, Ghana

Salary: Attractive