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Clinical trials & research

Clinical research

Clinical research takes a study from protocol development and ethics approval through site set-up, participant recruitment, monitoring, data management, safety reporting and final study results. Pharmacists can contribute across this entire process, working in research sites, hospitals, universities, pharmaceutical companies, contract research organisations and regulatory institutions.

A pharmacy background provides a strong foundation in medicines, patient care, clinical practice and scientific evaluation. These skills can support roles in clinical research coordination, clinical monitoring, investigational product management, pharmacovigilance, regulatory affairs, clinical data management, medical writing and clinical data analysis. Pharmacists may also contribute to protocol development, medication safety, participant education, randomisation and blinding, drug accountability, and the interpretation of clinical data.

Ghana has growing opportunities in this field. The Noguchi Memorial Institute at the University of Ghana, the Kumasi Centre for Collaborative Research, and the Kintampo, Dodowa and Navrongo Health Research Centres contribute to clinical research, with private facilities such as Ghana-Canada Medical Centre, while the Food and Drugs Authority regulates clinical trials nationally. Malaria, vaccines, infectious and non-infectious diseases and other public health priorities remain important areas of research activity. For many pharmacists, a Good Clinical Practice certification followed by experience as a study coordinator, research assistant or other entry-level research professional can provide a practical route into the field.

Key skills
Good Clinical Practice and research ethicsClinical research coordinationClinical data management and analysisPharmacovigilance and medication safetyRegulatory affairs and submissionsProtocol review and study documentationClinical monitoring and quality assuranceMedical and scientific writing
Next steps
  • Complete a Good Clinical Practice (GCP) certification
  • Learn a research data platform such as REDCap
  • Explore research roles in universities, teaching hospitals, research centres and CROs
  • Understand the FDA Ghana clinical trial approval process
  • Gain experience in research documentation, data management or pharmacovigilance
  • Apply for roles such as Research Assistant, Study Coordinator, Clinical Research Associate, Data Manager or Regulatory Associate
Related facilitators
Mark Ekow N. B. E. Bismarck
Mark Ekow N. B. E. Bismarck