- Design and implementation of medical and scientific strategies for the clinical development
- Evaluation of study results and securing medical plausibility and integrity of data
- Responsibility of the medical scientific site for overseeing the products and support of external in-licensing opportunities
- Granting of clinical knowledge on the preparation of documents for maintaining medicinal products and medical devices (investigator’s brochure, instructions for use, clinical evaluation reports)
- Participation of clinical study designs and liability of clinical study protocols and clinical study reports (according international regulations and guidelines)
- In charge of clinical sections for regulatory dossiers and medical aspects of interactions with regulatory authorities and notified bodies
- Exchange of scientific information with international and national experts
- Completed studies in medicine, give preference to PhD
- Knowledge of ICH-GCP, AMG, MED-DEV, MDR, and other relevant regulations
- Experience in clinical research and / or plastic surgery
- Expert knowledge of preparing and giving scientific presentations
- Team player, self-confident, strong communication and intercultural skills
- Fluent in business English
- Work in a multidisciplinary and international team
- A very renowned company
- Continuous trainings and possibilities to develop further
- A city with a high quality of life that perfectly embraces both modern and traditional values
- Our client is a very successful, in Germany founded company which offers not only an excellent market position, but also an exciting and dynamic working environment with flat hierarchies.
Reference number
386443/3
Contact
Phone:
+ 49 621 1788-4297
E-Mail:
positionen@hays.de
