Director, Site Management – Monitoring
Pfizer
full-time
Posted on:
Location Type: Remote
Location: Germany
Visit company websiteExplore more
Job Level
Tech Stack
About the role
- 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
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical researchmonitoringquality assuranceregulatory complianceGCPstudy strategiessite management
Soft Skills
leadershipcoachingcollaborationemployee development