Senior Clinical Affairs Manager (m/f/d)

You create independent clinical evaluations (CEP / CER) including the necessary research (literature, government reports etc.) and SSCPs You independently produce PMS/PMCF plans and associated reports (PMCF report, PMS report and PSUR) You work closely with external service providers (statisticians, clinical consultants etc.) You are responsible for the scientific support of our products as an interface between clinics, doctors, sales, development, product management, risk management and marketing You convey and pursue compliance with regulatory requirements, including their changes You provide clinical data and reviews for international authorisations You support the planning and supervision of clinical trials and evaluate them

You have successfully completed a medical, scientific or technical study or have a comparable qualification with corresponding additional qualifications You provide detailed knowledge of the legal and regulatory requirements in the field of the implementation, interpretation and publication of scientific studies in the medical environment, with In addition, you ideally have five years of professional experience and know each other with medical devices, but also ambitious career starters (m/w/d) give us a chance In addition to profound statistical knowledge, you can convince by your analytical skills You bring very good English skills and are safe in handling the office package You complete your profile through the ability to perceive problems, to develop structured solutions and to convey complex issues in interdisciplinary teams in a comprehensible way

Guests can enjoy a future-proof workstation at a modern location with an attractive remuneration. As a family-friendly company, we value that you can combine your professional and private goals and feel comfortable in the company. In addition to flexible working time, we support this through a wide range of social services, healthy placement and events outside the working day. .