Medical Writer / Scientific Advisor (m/f/d)

Your mission

• Creation of medical-scientific, clinical and regulatory content: Writing scientific contributions for leading international congresses (presentations, posters and abstracts), high-ranking publications with global reach on clinical studies and translational research projects, regulatory documentation (e.g. clinical study reports), annual scientific reports, newsletters, patient brochures, etc.
• Content development takes place in close cooperation with the departments Statistics/Bioinformatics and Medicine, as well as external national and international co-authors
• Coordination of internal and external communication for the technical content alignment of the contributions, as well as the technical publication process and submission of manuscripts and abstracts
• Collaboration on scientific projects including the option of independent evaluation and preparation of clinical and translational data
• Contribution to the creation of study protocols during planning new clinical studies
• Understanding and up-to-date knowledge of regulations, industry standards and company policies/procedures that are relevant to medical writing

Your profile

• You have successfully completed a medical or scientific degree in the field of life sciences (e.g. Medicine, life sciences) or a comparable education in the healthcare sector with corresponding experience
• You bring 3+ years of professional experience as a medical writer in similar environments
• You have medical/scientific knowledge in the field of oncology (ideally in gynecological oncology)
• You have a good understanding of medical and scientific concepts in order to present complex content correctly
• You have strong communication skills, analytical working methods and thinking skills, as well as good time and organizational management
• You are confident in using MS Office applications, software for managing literature references and graphic tools
• You can ideally have experience in using SPSS, R or SAS (desirable)
• You have very good written and spoken German and English skills
• You enjoy working independently in a young, dynamic and interdisciplinary team

Why us?

• Participation in exciting clinical studies and translational research projects with international attention
• An international working environment with regular exchange with other, internationally active study groups
• 30 days of vacation and an additional day off on December 24th and December 31st
• Work-life balance: trust-based working hours, flexible working hours, possibility of mobile working
• Numerous opportunities for further development: internal and external training
• Special services (e.g. JobRad, parking space, subsidy for the "Germany Ticket")
• Modern office space with very good accessibility
• Onboarding program with personal mentoring and digital learning program for a perfect start