Director, Site Management – Monitoring
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Job Description
Director of Site Management & Monitoring overseeing clinical studies in Germany for Pfizer. Leading teams to ensure compliance and quality in clinical trial management.
Responsibilities:
- Responsibility for site management and monitoring activities in Germany
- Functional and disciplinary leadership, including coaching of CRAs and other monitoring roles
- Ensuring quality, compliance and patient safety in accordance with GCP, regulatory requirements and internal standards
- Close collaboration with Study Start-Up, Regulatory, Medical Affairs, CROs and other internal and external partners
- Contributing to the development of country and site strategies
Requirements:
- Completed degree (e.g., natural sciences, medicine, pharmacy) or comparable qualification
- Several years of experience in clinical research, ideally within an international pharmaceutical company or CRO environment
- Leadership experience and an enthusiasm for developing employees are desirable
- Strong understanding of clinical study processes, monitoring, quality and regulatory requirements
- Fluent German and very good English skills
Benefits:
- Health insurance
- Professional development opportunities
- Flexible working hours
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