Job Description
Location: Innsbruck,,
Job Overview
We are seeking a seasoned Clinical Research Manager to spearhead the planning, execution, and completion of clinical studies in compliance with regulatory requirements.
- Develop and execute comprehensive study plans aligned with MDR, Declaration of Helsinki, and ISO 14155 regulations.
- Coordinate multicenter applications with authorities and ethics committees to ensure seamless project management.
- Contribute to the development of scientific publications and publication strategies.
- Prepare and manage safety reports to guarantee data integrity.
- Collaborate with cross-functional teams to drive process optimization, documentation improvement, and data preparation.
Key Responsibilities:
- Master’s degree or higher in Life Sciences.
- Minimum 2 years of experience as a Clinical Research Manager, preferably in medical devices.
- Profound knowledge of regulatory requirements in medical technology.
- Exceptional communication and project management skills.
- Proficiency in MS Office, review tools, reference management, and document management.
Benefits
This role offers a dynamic work environment, opportunities for professional growth and development, and a competitive compensation package based on qualifications and experience.
