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

You are actively involved in post-market monitoring and write the related documents such as PMS plans and PSURs You support the creation of clinical evaluations as required You independently develop opinions on specific scientific issues within the company You support other departments in writing test plans and reports Together with interdisciplinary teams, you will develop and test texts for product labelling

You have a completed scientific or medical degree You already have experience in scientific writing and the summary and evaluation of clinical studies and publications Fun You work conscientiously and in detail, but you recognize the connections and keep an overview CEP, CER, SSCP, PMS, PSUR, PMCF, MDR and MDCG are ideally not foreign words for you Searching in publicly accessible databases (e.g. Pubmed, MAUDE, etc.) do not cause any problems You convince with your strong communication and team skills The change between languages German and English in the Daily Business is of course for you

It is our agile and value-adding corporate culture with flat hierarchies and short decision-making paths that distinguish our dynamic and efficient work. All areas of responsibility act independently, characterized by our startup mentality combined with the structure and power of an established company. Through flexible working hours, regular team events, training and training opportunities, you can advance your development according to individual needs. .