Clinical Research Manager
vor 2 Monaten
Your Tasks- Plan and develop clinical investigations on medical devices, ensuring compliance with regulatory requirements and company procedures
- Oversee study activities, manage timelines, coordinate monitors, and work with clinical evaluation managers, data managers, and statisticians
- Manage study documentation and regulatory submissions, maintaining accurate and complete documentation, including protocols, informed consents, case report forms and study reports
- Liaise with study sites, investigators, and other internal and external stakeholders to facilitate the communication and ensure effective collaboration between all parties
- Contribute to the development of clinical strategies for successful launch and post-marketing clinical follow-up
- Your Profile- Masters’ degree or higher degree (University, FH) in Life or Natural Sciences, Healthcare or Medicine, Engineering or Technical Sciences
- Proven experience (min. 3 years) in clinical research, preferably in a medical device or pharmaceutical industry
- Very good English skills, both written and spoken; German skills are an advantage
- Strong project management and organizational skills, proactive attitude, excellent communication
- and interpersonal skills
- Willingness to travel internationally for clinical research activities and industry conferences (1-2 times per month on average)Your Benefits
- Central Location- Employee Discounts- Flexible Hours- International Environment- Onboarding- Workplace Well-Being- Further information
- Minimum Salary- Annual gross salary from
€ 55,670.28, based on professional qualification and experience.- Earliest Entry Date- This position is to be filled immediately.- Your Contact Person- If you have any questions please contact Marina Engl.
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