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.
go to method of application »
Method of Application