Senior Regulatory Medical Writer – Oncology (Hybrid/Remote)

A clinical stage biotech company is seeking a Senior Medical Writer to support the development of clinical and regulatory documents for antibody-drug conjugates (ADCs). You will collaborate with cross-functional teams, ensuring compliant document delivery throughout the drug development process. Ideal candidates will have a PhD or similar, alongside 3-5 years in medical writing and significant regulatory submission experience. This position can be based remotely within Germany or in Planegg, Bavaria. #J-18808-Ljbffr