Healthcare is an industry designed to help humans. As a global community, we continuously invest and commit to advancing human health. To deliver value and real outcomes. To rise to the challenge to find the next breakthrough by making the most of increasingly limited resources.
We are inspired by the potential and propelled by the possibilities. We share the vision to drive healthcare forward. To see how we can help accelerate progress and achievements. Others are developing these medical breakthroughs. We do our part by using breakthroughs in insights, technology and human intelligence to reimagine and deliver ways to help make them a reality.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.