2 Job Positions of Good Clinical Practices (GCP) Specialist at Rwanda Food And Drugs Authority (FDA) Under Statute: Deadline: May 20, 2024

0
743

Job responsibilities

ï‚§ Participate in planning and budgeting of the GCP inspections within the division ï‚§ Conduct GCP inspections for authorized clinical trial sites in the country using risk-based approach. ï‚§ Submit the GCP inspection findings to internal clinical trial committee for grading of GCP findings ï‚§ Prepare and submit GCP inspection reports for the inspected clinical trials and follow up on corrective and preventives actions (CAPA) ï‚§ Maintain and update a database for GCP inspections of clinical trials, ï‚§ Participate in the development and review of regulations, guidelines, training manuals, SOPs, IEC materials relevant to GCP inspection. ï‚§ Review and make recommendations for GCP inspection for regulatory actions. ï‚§ Develop and maintain good relations with customers in matters of good clinical practices inspection. ï‚§ Demonstrating the ability to consistently provide quality services that meet customer and regulatory requirements within their respective Office/Department/Division/ or Unit to meet Rwanda FDA quality objectives. ï‚§ Participating in organized training in Quality Management System. ï‚§ Doing the assigned tasks (job) by fully implementing the QMS established requirements.



Minimum qualifications
    • 1

      Bachelor’s Degree in Public Health

      3 Years of relevant experience


    • 2

      Bachelor’s Degree in Biomedical Engineering

      3 Years of relevant experience


    • 3

      Bachelor’s Degree in Pharmacy

      3 Years of relevant experience


    • 4

      Master’s Degree in Pharmacy

      1 Years of relevant experience


    • 5

      Bachelor’s Degree in Biology

      3 Years of relevant experience


    • 6.Bachelor’s Degree in Biotechnology

      3 Years of relevant experience


    • 7

      Master’s Degree in Biology

      1 Years of relevant experience


    • 8

      Master’s Degree in Biotechnology

      1 Years of relevant experience


    • 9

      Master’s Degree in Biomedical Engineering

      1 Years of relevant experience


    • 10

      Bachelor’s Degree in Pharmaceutical Sciences

      3 Years of relevant experience


    • 11

      Bachelor’s Degree in Molecular Biology

      3 Years of relevant experience


    • 12

      Master’s Degree in Molecular Biology

      1 Years of relevant experience


    • 13

      Bachelor’s Degree in Medicine

      3 Years of relevant experience


    • 14

      Master’s degree in Biomedical Sciences

      1 Years of relevant experience


    • 15

      Master’s Degree in Pharmaceutical Sciences

      1 Years of relevant experience


  • 16

    Bachelor’s Degree Biomedical Sciences

    3 Years of relevant experience


    Required competencies and key technical skills

      • 1
        Resource management skills

      • 2
        Problem solving skills

      • 3
        Decision making skills

      • 4
        Time management skills

      • 5
        Risk management skills

      • 6
        Results oriented

      • 7.Digital literacy skills

    • 8.Fluency in Kinyarwanda, English and/or French. Knowledge of all is an added advantage.

    Click here for more details & Apply











LEAVE A REPLY

Please enter your comment!
Please enter your name here