Senior Medical Advisor

vor 1 Tag

Neu Isenburg, Hessen, Deutschland GBG Forschungs GmbH Vollzeit
Why GBG?

Because here, with a dedicated team, flat hierarchies and room for your scientific vision, you can shape research that has a real clinical impact.

  • You will make a meaningful contribution to exciting clinical studies and research projects that attract international attention.
  • Enjoy a good work-life balance thanks to flexible working hours and the option of working from home two days per week. 
  • Numerous opportunities for your professional development.
  • Attractive benefits, including an employee support programme, JobRad, free parking, a Deutschland-Ticket subsidy and the option of a company pension scheme.
Would you like to help rethink clinical oncology? We look forward to receiving your application and getting to know you.The role

As a Senior Medical Advisor, you will ensure that our studies are medically sound, patient-centred and scientifically excellent. You will act as the primary medical contact for internal teams, trial centres and sponsors, playing an active role in the design, implementation and medical evaluation of clinical trials.

What we expect
  • A licence to practise medicine, with completed specialist training in gynaecology and obstetrics or internal medicine (ideally with experience in gynaecological or haematological oncology).
  • Extensive experience in clinical trials, with confidence in handling GCP, AE/SAE management, and medical documentation.
  • Enjoyment of clearly explaining complex medical issues and providing medical support to clinical teams.
  • The ability to work analytically and present scientific content accurately in writing.
  • Very good German and English skills, and confident use of digital tools such as MS Office, Teams and reference management software like EndNote.
The mission

Bring medical and scientific excellence to every phase of clinical research. You will develop and support the design of new studies, ensuring that concepts are clinically relevant, ethically sound, and safe for patients. At the same time, you will help generate valid, robust data that is scientifically and regulatorily convincing.

The tasks
  • Taking on medical responsibility within our studies: Your responsibilities will include evaluating protocols, defining inclusion/exclusion criteria and endpoints, reviewing reference documents, and ensuring the medical plausibility of all study steps.
  • Medical monitoring and safety: You will interpret AE/SAE reports, prepare safety-related assessments, and assist with the analysis of clinical risks for pharmacovigilance.
  • Supporting the operational study team: You will advise clinical research associates (CRAs) and project managers on protocol issues, deviations and medical queries, and ensure Good Clinical Practice (GCP)-compliant documentation.
  • Medical advice to trial centres: You will act as a medical contact person for investigators, accompany site training sessions and represent GBG at sub-board meetings with key opinion leaders.
  • Scientific work and reporting: You will review clinical data, prepare medical text contributions (CSRs, amendments and DSURs), and participate in manuscripts, conference contributions and publications, while also having the opportunity to work on your own scientific projects.

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