IQVIA
Compliance Clinical Trials
Nairobi • Kenya
Baker Hughes
Lab Technician
Nairobi • Kenya
UN-Habitat
Intern - Research and Report Writing
Nairobi • Kenya
Busara Center
Field Officer - KE
Nairobi • Kenya
Closed for applications
University of Nairobi
Research Assistant
Nairobi • Kenya
Closed for applications
Aga Khan Foundation
Enumerators – STRIDES Baseline Study
Nairobi • Kenya
Closed for applications
Aga Khan Hospitals
Research Assistant Nurse,iMAMA, Provost Office CoE
Nairobi • Kenya
Closed for applications
Rakai Health Sciences Program (Uganda)
Research Officer
Kalisizo • Uganda
Closed for applications
Maseno University
Research Assistant
Maseno • Kenya
Closed for applications
Get personalised job alerts directly to your inbox!
Transparency International Kenya
Research and Learning Officer
Nairobi • Kenya
Closed for applications
Companies hiring now
Aga Khan Foundation , Aga Khan Hospitals, IQVIA, Rakai Health Sciences Program (Uganda), TROPIKAL BRANDS (AFRIKA) LIMITEDProfession (Entry and Basic-level)
Accounting, finance, banking, insurance,Administrative, clerical,Agriculture, fishing, forestry, wildlife,Business, strategic management,Construction,Customer support, client care,Design, arts,Electrical engineering,Energy, power,Engineering, architecture,Food, nutrition,Government, community development, public services,Human resources,Information technology, software development, data,Installation, maintenance, repair,Legal,Manufacturing, operations, quality,Mechanical engineering,Media, communications, languages,Medical, health,Project, program management,Research, academy,Restaurant, hospitality, travel,Sales, marketing, promotion,Security,Skilled, manual labor,Sports, beauty, wellbeing,Teaching, training,Telecommunications,Transportation, logistics, driving,
Industry (Research, academy, Entry and Basic-level)
Seniority (Research, academy)
© Fuzu Ltd
IQVIA
Health care + 1 more
Description
Requirements
- Previous compliance experience within clinical trials required.
- Candidate must speak English
- Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH).
- Degree in life sciences or equivalent industry experience.
Please note: This role is not eligible for visa sponsorship and candidates must hold valid right to work for country of residence.
Responsibilities
- Document oversight - managing and organising essential trial documents (e.g., Trial Master File / TMF)
- Regulatory compliance support - ensuring studies follow guidelines like GCP (Good Clinical Practice), SOPs, and regulatory requirements
- Audit and inspection readiness - supporting preparation for audits or inspections from regulators (e.g., MHRA, FDA)
- Tracking and reporting - monitoring compliance metrics, deviations, and quality issues
- Process improvement - identifying gaps and helping improve compliance processes
Start hiring with Fuzu
Recruit better talent faster - on your own or with our support.
Explore recruitment platformJob search tips from Fuzu
Selected articles on cover letters, CV structure, and interview preparation.