Independent Clinical Monitor
AI summary
The NIHR GSU Ghana Hub is hiring an experienced Independent Clinical Monitor to oversee clinical research quality and compliance at the University for Development Studies (UDS), Tamale. The role involves monitoring clinical trials, ensuring adherence to GCP and FDA/Ghana Health Service requirements, and supporting site activation and reporting. Full-time position based in Tamale and the Northern Region.
- Mid-level clinical monitoring role with 3–5 years required experience
- Based at UDS Tamale, Northern Region, Ghana
- Requires GCP certification and health sciences degree
- Involves travel to study sites and regulatory reporting
- Competitive salary and professional development opportunities
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?
- Required3+ 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 monitor, clinical research, complianceThe 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 Independent Clinical Monitor 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 monitor, clinical research, compliance, 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 Independent Clinical Monitor role in monitor, clinical research?
- 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
Independent Clinical Monitor
NIHR GSU Ghana Hub
Medical & Pharmaceutical
Today
Easy apply
New
Tamale & Northern Region
Full Time
Healthcare
Confidential
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Job summary
We are seeking a highly experienced and detail-oriented Independent Clinical Monitor to oversee the quality and compliance of clinical research activities at the University for Development Studies (UDS), Tamale. The successful candidate will ensure that clinical trials are conducted in accordance with Good Clinical Practice (GCP) guidelines, study protocols, and the regulatory
Requirements
- of the Food and Drugs Authority (FDA) Ghana, Ghana Health Service (GHS), and the Christian Health Association of Ghana (CHAG).
- Min Qualification:
- Degree
- Key
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 &
- 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
- in clinical research monitoring, clinical trial management, or a related role.
- working with regulatory bodies such as FDA Ghana, Ghana Health Service, or CHAG is an added advantage.
- Skills & Competencies:
- 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.
- What We Offer:
- 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
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Responsibilities
- 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.
- Qualifications &