Medical Writer / PMS Coordinator (m/f/d)

You are actively involved in post-market surveillance and prepare the associated documents, such as PMS plans and PSURs.

You provide support as needed in the creation of clinical evaluations.

You independently develop statements on specific scientific questions within the company.

You assist other departments in writing test plans and reports.

Together with interdisciplinary teams, you draft and review texts for product labeling.

You have a completed degree in a scientific or medical field.

You already have experience in scientific writing, and you enjoy summarizing and evaluating clinical studies and publications.

You work diligently and with attention to detail, while still recognizing the bigger picture and maintaining an overview.

CEP, CER, SSCP, PMS, PSUR, PMCF, MDR, and MDCG are ideally not foreign terms to you.

Conducting research in publicly accessible databases (e.g., PubMed, MAUDE, etc.) is no problem for you.

You impress with your strong communication and teamwork skills.

Switching between German and English in your daily business is second nature to you.