Opportunities & Vacancies

Welcome to our Opportunities and Vacancies Page! 

In order to carry out its duties in research, training, and treatment in the area of tropical medicine, KCCR offers a number of jobs. You desire to join us? Below are all of our open positions right now.

VACANCY NOTICE – Quality Assurance Officer

JOB LOCATION – Kumasi

Position

The management of the Kumasi Centre for Collaborative Research in Tropical Medicine (KCCR), together with the Global Health and Infectious Diseases Research Group (GHID), is seeking a Quality Assurance Officer to join our interdisciplinary team.

 

GHID conducts cross-cutting research in global health and infectious diseases, providing actionable insights to reduce disease burden in Ghana and beyond.

 

The successful candidate will establish, monitor, and improve continuously the Quality Management System to ensure compliance of Research staff and procedures with International Regulatory and Ethical requirements as well as Good Clinical Practices (GCP) and Good Clinical Practice (GCLP) toward ensuring the safety of study participants and the integrity of biological material and data.

Main Responsibilities/Activities

·         Develop and maintain GCP/ICH compliant processes which control the quality of work and clinical researchs conducted by:

o   Develop and deliver training programs to enhance awareness of quality requirements and best practices among clinical research personnel to ensure compliance with regulatory standards and guidelines where applicable.

o   Conduct and assist in internal audits and inspections to identify gaps,assess compliance with SOPs and applicable regulations.

·         Support in the design of all study protocols, standard operating procedures (SOP), study specific procedures and study forms. Ensure adequate training to team members.

·         Participate in the review and installation of technology products and equipment. Ensure appropriate equipment SOP and training are in place and ensure good maintenance of the equipment.

·         Ensure the proper documentation of quality-related activities, including audit findings, corrective and preventive actions, and risk assessments.

·         Prepare and present quality reports and metrics to management, highlighting key findings, trends, and areas for improvement.

·         Perform on-call duties in accordance with the requirements of the research activities.

–          Support in reporting (results and analysis) on specific topics for general and scientific dissemination.

 

Required Qualification, Competencies and Professional Experience

  • Qualifications
  • Bachelor’s Degree or equivalent experience in the Life sciences (i.e., Pharmacy, Biochemistry, Biological Science, Microbiology, Medical Lab technology, Nursing etc.) or associated functional discipline.
  • Research experience

 

  • Competencies and Professional Experience
  • Minimum of three years of experience in Quality Assurance of clinical research studies.
  • Proficiency in using quality management systems and tools.
  • Strong ability to use initiative, prioritize, multi-task, and work well under pressure to meet deadlines.
  • Clear and systematic thinking demonstrates good judgment and problem-solving competencies.
  • Excellent attention to detail and a meticulous approach to quality assurance processes.
  • Strong communication skills in multicultural, multi-lingual environments.
  • Strong ability to provide high level support in project/program delivery.
  • Strong organizational skills to maintain and manage documentation related to quality assurance processes.
  • Proven ability to work effectively in a team environment and matrix structure.
  • Thorough understanding of local regulatory requirements and international guidelines, such as Good Clinical Practice (GCP), Good Clinical Laboratory practice (GCLP) and ISO where applicable.

 

  • Desired Attributes
  • Very good knowledge of Microsoft Office Suite and Computer literacy
  • Experience in clinical trials is an advantage.

 


Remuneration will be according to KCCR standards. The contract will be for a period of 12 months (renewable) with the first 3 months as probation.

Expected start date: June 2025.

 

MODE OF APPLICATION

Interested persons should email their applications addressed to The Head of Administration, KCCR, KNUST, Kumasi including their CV, motivation letters, and copies of certificates to: info@kccr.de with e.matey@kccr.de and ghid@kccr.de copied.

Closing Date: 12th May 2025. Only shortlisted applicants will be contacted. 

For further information on the position, please contact e.matey@kccr.de.