Global Medical Writer
Novo Nordisk A/S
Bangalore, India
3d ago

Are you a proven leader who can set direction and drive team performance? Do you have expertise in the field of medical communication?

Then we might have the right position for you. We are looking for a Team Lead who is excited about joining a growing team, working in an international environment.

About the department

Global Medical Affairs, GBS (GMA GBS) is an extension of the Global Medical Affairs unit in Headquarters (HQ) in Denmark, is based out of Global Business Services (GBS), Bangalore, India.

One of the team within GMA-GBS is Scientific Communications Content Hub team. The team consists of highly motivated global scientific advisor, medical writer, publication manager and medical illustrator working together with medical affairs organizations across the globe - International Operations strategic office (IO-SO), Zurich, Switzerland, regional medical affairs units namely Asia Pacific (APAC) based at Dubai, North West Europe (NWE) based at Copenhagen, Denmark

  • Our core competencies are communicating scientific and medical knowledge on our products to the external scientific community and across the organization;
  • delivering external medical events including in-house content development and project management and publication planning

    The position

    As a medical writer, you are in charge for performing medical writing tasks in collaboration with GMAB medical affairs department.

    You will be expected to contribute to knowledge sharing and good collaboration with stakeholders and colleagues world-wide.

    Above all, your experience working with global stakeholders and cross functional teams will help you to collaborate successfully in this role.

    You are required to have good communication and analytical skills, experience in publication writing and strong understanding of publication guidelines

    Qualifications

    We expect you to be graduate (PhD, MSc., M Pharm, MD, DDS, DVM or equivalent) and has the below qualifications :

  • 6 years of experience with scientific research methodology, including designing and conducting experiments, and analysing and reporting experimental results
  • Experience with scientific writing in English (publications for peer reviewed journals or equivalent)
  • Experience working within a global setting
  • Strong understanding of external requirements, guidelines and regulations governing publication writing
  • Experience from the pharmaceutical / CRO industry
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