"Uncover Your Dream Career as an Associate Medical Writer with Novo Nordisk!"
"Uncover Your Dream Career as an Associate Medical Writer with Novo Nordisk!"

Associate Medical Writer Novo Nordisk! Pharma Apply Online

Associate Medical Writer

Category: Medical Affairs

Location: Bangalore, Karnataka, IN

Department: Global Medical Affairs – Global Business Services (GMA – GBS).

Are you passionate about medical writing? Do you want to contribute to life-changing scientific activities on a global scale? We are looking for an Associate Medical Writer to join our Global Medical Affairs unit. If this excites you, then apply today for a life-changing career.

The Position

As an Associate Medical Writer at Novo Nordisk, you will:

  • Moderate discussions with study groups for the development of study protocol and/or study report.
  • Facilitate document-review meetings and provide comments on consolidated documents.
  • Coordinate the clinical document version reviews and approval processes.
  • Ensure audit preparedness.
  • Perform literature searches and prepare summaries of systematic literature searches.
  • Participate in internal/external marketing/medical activities, such as expert meetings, lectures, and conferences.
  • Contribute to ongoing improvements in cross-functional and global collaboration and sharing of better practices and knowledge.
  • Maintain up-to-date knowledge and competencies within relevant therapeutic and professional areas.
  • Perform medical writing tasks (study protocol and study report) in collaboration with global medical directors.
  • Prepare study protocols, non-interventional study reports, and investigator’s brochures as per SOPs, timelines, guidelines, and regulatory requirements.
  • Develop abstracts, congress posters, and presentations.
  • Create publication proposals in line with the standard NN template.
  • Maintain a good working relationship with stakeholders and colleagues.

Qualifications

  • A degree in a relevant field (e.g., life sciences, medical, pharmaceutical).
  • 2+ years of experience in medical writing, particularly in preparing study protocols, non-interventional study reports, and investigator’s brochures.
  • Good understanding of real-world studies and therapy areas (diabetes/obesity/MASH).
  • Strong ability to perform literature searches and prepare summaries.
  • Experience in developing abstracts, congress posters, and presentations.
  • Excellent communication and collaboration skills.
  • Ability to ensure audit preparedness and manage clinical document version reviews and approval processes.
  • Experience in the pharmaceutical or healthcare industry.
  • Familiarity with regulatory requirements and guidelines.
  • Experience in process improvements and knowledge sharing.

Deadline: 15 October 2024.

To apply for this exciting opportunity, visit this link

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