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About the role
Key responsibilities & impact- You are responsible for implementing global studies in Germany
- You work closely with your local CRA colleagues within various study teams
- You oversee a selection of investigational sites and manage collaboration with partners and regulatory authorities
- You ensure that all internal and external requirements and standards are met in your projects
Requirements
What you’ll need- Bachelor's degree or equivalent qualification, ideally in a health-related field (e.g., Medicine, Life Sciences, Pharmacy)
- At least 2 years of on-site and remote monitoring experience in clinical trials (phases 1–4)
- Solid knowledge of relevant regulations and standards
- Strong planning skills, excellent organizational abilities, and analytical thinking
- Excellent interpersonal skills and the ability to reflect on your work
- Business-fluent German and English
Benefits
Comp & perks- Opportunity to help shape modern clinical research in a responsible role
- An agile and supportive team
- An employer already recognized as a “Top Employer”
- Possibility of long-term collaboration with good performance and successful integration into the team
- Support as you begin your journey at AbbVie
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 TrialsOn-Site MonitoringRemote MonitoringRegulations KnowledgeAnalytical Thinking
Soft Skills
Planning SkillsOrganizational Abilities