Clinical Trial Project Manager
AI summary
NIHR GSU Ghana Hub is hiring an experienced Clinical Trial Project Manager based at the University for Development Studies, Tamale Campus. The role involves planning, coordinating, and overseeing clinical research projects across multiple sites, ensuring compliance with protocols, GCP, and regulatory requirements. Full-time position with an attractive salary for candidates with a health-related degree and at least four years of relevant experience.
- Full-time role based at UDS Tamale Campus in Northern Ghana
- Requires a degree in Clinical Research, Public Health, Health Sciences, Medicine, Nursing, Pharmacy, or related field
- Minimum 4 years of clinical trial or health research project experience needed
- Attractive salary with travel to participating research sites required
- Focus on GCP compliance, multi-site coordination, and stakeholder management
AI job guide
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AI salary guide
Source salary availableThe source lists Attractive. Confirm the final pay, benefits, contract terms and allowances directly with the employer before accepting an offer.
Can you qualify for this role?
- Required4+ years of relevant experienceThe job post includes a minimum experience signal.
- RequiredEducation or certification mentioned in the postThe captured text mentions education, a diploma, certificate, or licence.
- PreferredPractical evidence in entregador, finance, Project ManagerThe tags and summary point to skills connected with this role.
- RequiredAvailability to work in TamaleThe vacancy is associated with this location.
- UnclearComfort with the Full Time contract termsConfirm hours, duration, probation and benefits at the original source.
Documents to prepare
- Likely requiredUpdated CV
- Role specificCover letter or short employer message
- OptionalProfessional references
- Role specificAcademic or professional certificates
- VerifyID or passport only after verifying the employer
Application tips for this job
- Place your strongest Clinical Trial Project Manager evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to NIHR GSU Ghana Hub and the role in Tamale.
- Add concrete examples related to entregador, finance, Project Manager, ideally with measurable outcomes or clear responsibilities.
- Follow the instructions from Jobberman Ghana; avoid sending documents to unofficial contacts or copied links.
- Confirm the deadline, interview location and employer contact before sharing personal documents.
Source and safety check
- Jobberman Ghana
- Original source link available
- Application method is clear
- Deadline not specified
- No major risk signal was detected in the captured text.
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Interview preparation
- What experience makes you a strong fit for this Clinical Trial Project Manager role in entregador, finance?
- How have you handled responsibilities similar to those in this job post?
- Are you available to work in Tamale under the listed contract or schedule?
- Prepare examples with clear responsibilities, tools used and measurable outcomes.
- Review the source and research NIHR GSU Ghana Hub before the interview.
Ask what the first priorities will be in the role and how success will be measured.
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Original source description
Clinical Trial Project Manager
NIHR GSU Ghana Hub
Medical & Pharmaceutical
Today
Easy apply
New
Tamale & Northern Region
Full Time
Healthcare
Confidential
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Job summary
NIHR GSU Ghana Hub is seeking an experienced and highly organized Clinical Trial Project Manager to oversee the planning, coordination, and delivery of clinical research projects and trials. The successful candidate will coordinate trial activities across participating research sites, work closely with investigators and research teams, monitor project progress, and ensure that studies are delivered according to approved protocols, timelines, quality standards, and applicable regulatory requirements.
Min Qualification:
Degree
Experience
- Level:
- Mid level
- Length:
- 4 years
- Language Requirement:
- English
- Working Hours:
- Full Time - 8 to 5
- Applicant
- Location:
- Tamale & Northern Region, Ghana
- Job descriptions &
- managing or coordinating clinical trials or health research projects.
- Good understanding of Good Clinical Practice (GCP) and clinical research processes.
- 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.
- working with clinical research teams, hospitals, universities, or research institutions is an advantage.
- with multi-site clinical trials.
- Knowledge of Ghanaian clinical research and regulatory requirements.
- preparing research reports and regulatory documentation.
- Strong stakeholder and team management skills.
- Ability to travel to participating research sites when required.
- Key Competencies
- 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
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Requirements
- Key
- & Qualifications
- Bachelor's or Master's degree in Clinical Research, Public Health, Health Sciences, Medicine, Nursing, Pharmacy, Project Management, or a related field.
- Previous
Responsibilities
- 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.
Preferred Qualifications
- Skills
- Clinical trial project management experience.