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Doctor (all genders) for scientific research

GBG Forschungs GmbH

Neu-Isenburg

Hybrid

EUR 60.000 - 85.000

Vollzeit

Vor 24 Tagen

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Zusammenfassung

A leading clinical research company seeks a medical professional to supervise clinical studies and ensure patient safety. The ideal candidate will have a degree in human medicine or pharmacy, with a strong focus on oncology. This role offers the opportunity to participate in exciting projects and develop further in an international environment, with flexible working conditions.

Leistungen

Flexible working hours
Partial remote working option
Job-Bike
Parking space
Subsidy for the 'Germany Ticket'

Qualifikationen

  • Completed training in gynecology & obstetrics or internal medicine.
  • Experience with scientific work and clinical trials is essential.
  • Fluent in German and English (written and spoken).

Aufgaben

  • Supervise clinical studies ensuring patient safety and medical monitoring.
  • Draft study protocols and clinical study reports.
  • Collaborate on international congress contributions and publications.

Kenntnisse

Strong communication skills
Analytical thinking
Organizational skills
Time management
Tech savvy

Ausbildung

Degree in human medicine
Specialist training in gynecology & obstetrics or internal medicine
Degree in pharmacy

Tools

MS Office applications
MS Teams
Reference management software (e.g. EndNote)

Jobbeschreibung

Your mission
  • Supervising clinical studies with responsibility for the medical content and patient safety, including medical monitoring, pharmacovigilance and evaluation of reference documents
  • Giving medical advice to external study physicians and internal project partners on all studies and projects conducted by GBG
  • Planning and drafting study protocols and amendments, writing clinical study reports and development safety update reports
  • Collaborating in scientific contributions for leading international congresses and publications with global reach on clinical studies and translational research projects
  • Opportunity to conduct and publish your own scientific work
  • Regular active participation in our subboard meetings with external key opinion leaders
  • Regular active participation in internal and external training events, including speaking engagements

Your profile
  • You have successfully completed a degree in human medicine and have completed specialist training in gynecology & obstetrics or internal medicine - ideally with experience in gynecologic oncology and/or hemato-oncology
  • Alternatively, you have successfully completed a degree in pharmacy and have relevant experience in the conduct of pharmaceutical trials in oncology
  • You have experience with scientific work and clinical trials including work according to Good Clinical Practice (GCP)
  • You enjoy working independently in a highly motivated and dynamic team
  • You have the following skills: strong communication skills, analytical working and thinking skills, as well as a very good organizational and time management
  • You are tech savvy and confident in using MS Office applications, as well as MS Teams and reference management software (e.g. EndNote)
  • You have a very good command of written and spoken German and English

Why us?
  • Participation in exciting clinical trials and translational research projects with global reach
  • An international working environment with regular exchange with other internationally active study groups
  • Work-life balance: trust-based and flexible working hours, option for partial remote working
  • Numerous opportunities for further development in internal and external trainings
  • Special services (e.g. Job-Bike, parking space, subsidy for the "Germany Ticket")
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