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Clinical Research Medical Advisor

vor 3 Monaten


Neu Isenburg, Hessen, Deutschland GBG Forschungs GmbH Vollzeit

Enhance Clinical Research – At GBG Forschungs GmbH, we merge academic insights with medical proficiency to foster economic adaptability.

As an independent and unbiased academic research organization (ARO), we are dedicated to the development, execution, and assessment of clinical study initiatives aimed at enhancing treatment options for breast cancer patients. Our collaborators encompass a diverse range of entities from academia, research, and industry. With a workforce of approximately 140 professionals, our headquarters is situated in Neu-Isenburg.

We provide a profound connection to scientific and study initiatives, alongside a stimulating and diverse professional landscape with promising growth opportunities.

Your Key Responsibilities

  • Overseeing clinical trials with a focus on medical integrity and patient safety, including medical oversight, pharmacovigilance, and review of reference materials.
  • Providing medical guidance to external study physicians and internal project stakeholders regarding all studies and initiatives managed by GBG.
  • Designing and drafting study protocols and amendments, as well as composing clinical study reports and development safety update reports.
  • Contributing to scientific presentations for prominent international conferences and publications with a global impact on clinical studies and translational research.
  • Opportunity to conduct and disseminate your own scientific research.
  • Regular engagement in our subboard meetings with external key opinion leaders.
  • Active participation in both internal and external training sessions, including opportunities for public speaking.

Your Qualifications

  • A completed degree in human medicine with specialization in gynecology & obstetrics or internal medicine, preferably with experience in gynecologic oncology and/or hemato-oncology.
  • Alternatively, a degree in pharmacy with relevant experience in conducting pharmaceutical trials in oncology.
  • Experience in scientific research and clinical trials, adhering to Good Clinical Practice (GCP) standards.
  • Adept at working independently within a highly motivated and dynamic team environment.
  • Possess strong communication, analytical thinking, and exceptional organizational and time management skills.
  • Proficient in MS Office applications, MS Teams, and reference management software (e.g., EndNote).
  • Fluent in both written and spoken German and English.

What We Provide

  • Engagement in exciting clinical trials and translational research projects with a global perspective.
  • An international work environment with regular collaboration with other globally active study groups.
  • Work-life balance: flexible working hours based on trust, with options for partial remote work.
  • Numerous opportunities for professional development through internal and external training programs.
  • Additional benefits such as a Job-Bike, complimentary parking, public transportation subsidies, and lunch provisions.

We invite you to explore a role within a dynamic organization characterized by short decision-making processes and a committed team. Innovation and dedication are the hallmarks of our collaboration.