Beschreibung
For one of our Pharma-clients in Hessen we are seeking freelance support as:
Medial Writer Lead (M/F/*)
Tasks:
• Oversee and coordinate the preparation of documentation for regulatory submissions (e.g., investigator brochures, protocols, and clinical study reports) in collaboration with other team members or CROs
• Write strategic submission documents (e.g., IMPDs, briefing documents, clinical summaries)
• Ensure the quality of documents
Qualifications:
• Master or Ph.D. in the scientific area (Oncology)
• Experience in Medical Writing in the area of Oncology (min. 2-3 years)
• Experience with regulatory submissions
• Experience with CROs
• Experience with clinical and non-clinical studies
• Experience with local/regional studies, manuscripts, promotion writing, clinical assumptions
• Business fluent in English, German is only nice to have
Frame Data:
• Start: 01.02.21, latest 15.02.21
• Duration: 31.01.2022
• Capacity: full-time, remote