Description
Interim Clinical Affairs Manager (60% - 80%) (m/f)
Reference: -en
Start: asap
Duration: 3 MM++
Main tasks:
- Support cross-functional assessments of all potential clinical studies (pre- and post-market) and the regulatory requirements for such studies
- Provide strategic input and execution of clinical trials from protocol design to the final clinical study report for specified studies
- Oversee and provide guidance on the development of study documents and study management, e.g. CIP, ICF, CRF, data management plan and quality review and tracking.
- Ensure conformity to ISO 14155, national laws, and applicable regulatory standards, by working with the applicable functional areas as needed.
- Perform clinical project management duties, leading pre and post market clinical studies as required.
Main qualifications
- Degree in Life Sciences or equivalent education
- Experience in Clinical Affairs or Clinical Project Management
- English is a must have. German is a plus
- Experience with Medical Devices Class II or III
- Organizational skills and team spirit
Main advantages:
- You will work in an international environment
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.