Director, Early Development Regulatory Lead - Garching bei München
vor 1 Woche
Job summary
We would like to fill the following permanent vacancy in a hybrid working model in Garching as soon as possible. Serve as Regulatory Affairs expert for early-stage development projects within the radiopharmaceutical pipeline with primary focus on upcoming IND/CTA submissions reporting directly to the Head of Clinical Regulatory Affairs.
Responsibilities
- Serve as Regulatory Affairs expert for early-stage development projects within the radiopharmaceutical pipeline with primary focus on upcoming IND/CTA submissions.
- Act as the primary regulatory contact with key Health Authorities (FDA, EMA)
Stellenbeschreibung
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