• Application Deadline:
• Position: Compliance Clinical Trials Assistant



• Job Type Full Time



• Qualification BA/BSc/HND



• Experience



• Location Abuja




• Job Field Medical / Healthcare 
  
  

About the job

• We are seeking an experienced Compliance Clinical Trials Assistant to join our cFSP (sponsor-dedicated) team in EMEA.


• Candidates are required to have previous compliance experience within clinical trials to be considered.

Key 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

What We’re Looking For

• 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.