Clinical Trial Project Manager

• Plan, coordinate, and oversee clinical trial activities from initiation through completion.
• Develop and monitor project timelines, milestones, deliverables, and budgets.
• Coordinate activities between the Ghana Hub, principal investigators, research teams, and participating clinical sites.
• Support site initiation, site activation, recruitment, monitoring, and trial close-out activities.
• Monitor recruitment progress and identify potential risks or delays.
• Ensure trial activities are conducted in accordance with approved protocols, Good Clinical Practice (GCP), and applicable regulatory requirements.
• Coordinate training and meetings for research staff and participating sites.
• Maintain accurate trial documentation and project records.
• Prepare regular project progress reports and updates for relevant stakeholders.
• Identify, document, and escalate project risks and issues.
• Work closely with data, finance, regulatory, and clinical teams to ensure effective trial delivery.
• Liaise with relevant regulatory and institutional stakeholders where required.
• Support preparation for monitoring visits, audits, and regulatory inspections.
• Ensure timely communication and follow-up on project action points.
• Contribute to the preparation of study reports, presentations, and other project documentation.

• Bachelor's or Master's degree in Clinical Research, Public Health, Health Sciences, Medicine, Nursing, Pharmacy, Project Management, or a related field.
• Previous experience managing or coordinating clinical trials or health research projects.
• Good understanding of Good Clinical Practice (GCP) and clinical research processes.
• Experience coordinating multiple stakeholders and research sites.
• Strong project planning, organizational, and time-management skills.
• Excellent written and verbal communication skills.
• Strong analytical and problem-solving abilities.
• Proficiency in Microsoft Office and project management tools.
• Ability to manage multiple priorities and meet deadlines.
• Experience working with clinical research teams, hospitals, universities, or research institutions is an advantage.

• Clinical trial project management experience.
• Experience with multi-site clinical trials.
• Knowledge of Ghanaian clinical research and regulatory requirements.
• Experience preparing research reports and regulatory documentation.
• Strong stakeholder and team management skills.
• Ability to travel to participating research sites when required.

• Project management
• Clinical research coordination
• Leadership and teamwork
• Attention to detail
• Risk management
• Communication and stakeholder engagement
• Problem-solving
• Time management
• Compliance and quality assurance

Location: University for Development Studies (UDS), Tamale Campus, Tamale

Salary: Attractive