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
About us
Clinical research under better conditions - We combine academic knowledge and medical expertise with economic flexibility.
GBG Forschungs GmbH is an independent and academic research institute (ARO) that develops, conducts and evaluates clinical study projects to improve the treatment options for breast cancer. Our cooperation partners include companies and organizations from science, research and industry. The company, based in Neu-Isenburg, currently employs around 140 people.
GBG Forschungs GmbH offers you a high level of identification with scientific and study projects. In addition, you will benefit from an exciting and varied field of activity with attractive development prospects.
In total, more than 68,000 patients have been included in GBG studies to date. These range from important academic registry studies to international approval studies of drugs with approx. 200 to 400 centres. Become part of our team and help shape the future of breast cancer research!
We are looking for committed and talented candidates who would like to strengthen our team and shape the future of breast cancer research together with us. If you find yourself in our requirements profile, send us an application!
