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...
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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.
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