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Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- 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
What you’ll need- 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
Comp & perks- Health insurance
- Professional development opportunities
- Flexible working hours
ATS Keywords
✓ Tailor your resumeApplicant 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