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Compliance Clinical Trials Assistant – Clinical Research
IQVIA · Algiers
Description du poste
About the role
IQVIA is looking for a Compliance Clinical Trials Assistant to support its sponsor‑dedicated team across EMEA. The role focuses on ensuring trial documentation and processes meet regulatory standards and quality expectations.
Key responsibilities
- Manage and organise essential trial documents, including the Trial Master File (TMF).
- Support regulatory compliance by applying GCP, SOPs, and other relevant guidelines.
- Assist in audit and inspection readiness for regulators such as MHRA and FDA.
- Track and report compliance metrics, deviations, and quality issues.
- Identify gaps and contribute to process‑improvement initiatives.
Required profile
- Previous compliance experience within clinical trials.
- Fluent in English.
- Knowledge of Good Clinical Practice (GCP) and ICH guidelines.
- Degree in life sciences or equivalent industry experience.
- Valid right to work in the country of residence (no visa sponsorship).
Required skills
- Good Clinical Practice (GCP)
- International Conference on Harmonisation (ICH) regulations
- Trial Master File (TMF) management
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IQVIA
Algiers
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