Medical Advisor @ Grünenthal Group

  • TypeFull Time
  • SeniorityLeadership
  • RoleNon-Clinical
  • SectorNon-Clinical
  • LocationUK

If you’re passionate about changing lives for the better, this is the opportunity you’ve been waiting for. In Research & Development, we’re continuously exploring innovative new treatment options to make a stronger, more positive impact on the lives of the patients we serve. You’ll work with talented colleagues in a state-of-the-art Research & Development environment, developing innovative medicines that change the live of patients for the better and help us make progress towards our vision of a world free of pain. Join us today, and discover the difference you can make.


What The Job Looks Like

  • Support Medical Affairs in the cluster area in coordination with the global medical affairs team in the launch process of a new product in pain therapy.
  • Field-based work & support in order to achieve company’s goals
  • Identify key medical science information & insights, market opportunities and threats in the area of osteoarthritis and its pain management, inspired by contacts/needs assessments with health care professionals/KEE and by other external stakeholders, and provide relevant feedback to the management team (Medical Affairs/Marketing/Market Access), so to help appropriate strategic decision making
  • Implement medical projects and activities in line with the Cluster Medical Affairs & Global strategy team including, medical education programs, Investigator Initiated Trials (IITs) and Real-World Evidence (RWE) data generation, in compliance within the overall company quality principles, values, and applicable policies of GRT and local rules and regulations
  • Be responsible supporting for managing specific projects in agreement with/as directed by the Medical Manager/Director and ensure all feedback on relevant matters is relayed to the Medical Manager
  • Attend OA related relevant scientific meetings and congresses
  • Support/Conduct internal trainings on medically relevant topics related to osteoarthritis.
  • Report Adverse Drug Reactions (ADRs) and product quality issues to GRT regulatory staff according to local laws
  • Develop and maintain ongoing relationships with Key External Experts, HCPs, Scientific Societies, Patient Associations and other entities, and facilitate appropriate medical and scientific information exchange

What You’ll Bring To The Table

  • MD or Bachelor degree in Health Sciences or related discipline with a good working knowledge in presenting data in hospitals or other functions.
  • Experience in Medical Affairs and/or Medical Information areas is an advantage
  • Ideally some field-based pharmaceutical experience
  • Will need to have the ability to travel as a guide 50% in the cluster countries (UK, Ireland, Nordic countries)