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Nationality
Any Nationality
Gender
Not Mentioned
Vacancy
1 Vacancy
Job Description
Roles & Responsibilities
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.
- 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.
Desired Candidate Profile
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.
Company Industry
- Consulting
- Management Consulting
- Advisory Services
Department / Functional Area
- Administration
Keywords
- Compliance Clinical Trials Assistant
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iqvia
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
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