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Ihre Aufgaben
Ihr Profil
* Bitte ersetzen
* Definition of product strategies
* Specification of new products
* Assistance in the market entry
* Assistance in the market entry
* Bitte ersetzen
* Definition of product strategies
* Specification of new products
* Assistance in the market entry
* Assistance in the market entry
Haben wir Ihr Interesse geweckt? Dann bewerben Sie sich bitte online! Wir freuen uns auf Sie.
The Medical Affairs Group is responsible for the design, conduction and evaluation of international first-in-man, regulatory submission and post-marketing trials.
Your Responsibilities Your Profile
* Leading discussions and negotiations with notified bodies and authorities to discuss clinical strategy for the approval of our products
* Take ownership and responsibility in providing scientific/ clinical input into the phases of product development steps as defined in procedure
* Planning and writing of clinical evaluation reports taking into account current laws and regulations
* Interact with different departments and functions including R&D, RA, Risk and Validation, clinical study managers, biostatisticians and clinical investigators
* PhD/MD in medicine, life or health sciences
* At least 5 years experience in medical writing, with minimum of 3 years in medical device or pharma industry
* Ability to interpret complex clinical data and good knowledge and understanding of statistics
* Experience with conducting extensive medical literature searches and reviews using various database sources such as PubMed
* Team oriented, confident and proactive personality with an analytical working style
* Excellent command of spoken and written English and German
Are you interested? Please apply online! We are looking forward to welcoming you.
Standort: 6901
Arbeitszeit: Vollzeit
Vertragsart: befristet
Erreichbare Entgeltgruppe: EG09
Kennziffer: 6261
Abteilung:
Ansprechpartner HR: Recruiting Specialist TU
Tel.:
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