Associate Director Clinical Compliance ensuring CD operates according to quality standards and health regulations. Collaborating on audits, training, and continuous quality improvement efforts.
About the role
- Regulatory Specialist managing site activation and compliance for clinical trials at IQVIA. Responsible for regulatory documents and project timelines ensuring adherence to operational procedures.
Responsibilities
- Effectuer les tâches au niveau national associées aux activités d’activation de sites (AS) conformément à la réglementation locale et/ou internationale applicable.
- Sous supervision générale, servir de point de contact unique (PCU) pour les centres de recherche.
- Veiller au respect des procédures opérationnelles normalisées (PON).
Requirements
- 1 an d’expérience en recherche clinique.
- Combinaison équivalente d’études, de formation et d’expérience.
Benefits
- Des régimes d’incitation, des primes et/ou d’autres formes de rémunération peuvent être proposés, en plus d’une gamme d’avantages sociaux liés à la santé, au bien-être et/ou d’autres bénéfices.
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