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[Freshers] Eli Lilly Hiring in Medical Writing

Job Title: Medical Writer, Medical Affairs
Location: Bangalore, Karnataka, India
Category: Medical
Employment Type: Full Time, Regular

About Us:
At Lilly, we are driven by our commitment to unite caring with discovery to enhance lives globally. Headquartered in Indianapolis, Indiana, we are a leading global healthcare company dedicated to developing life-changing medicines, advancing disease understanding, and contributing to our communities through philanthropy and volunteerism. Our mission is to make a meaningful difference in the lives of people worldwide, placing people at the forefront of everything we do.

Purpose:
Scientific data and information form the cornerstone of our work at Lilly. Providing accurate, balanced, and timely information to regulators, healthcare professionals, patients, and other stakeholders throughout the drug development lifecycle is crucial. In an era where healthcare providers are inundated with data and navigating complex systems, Lilly Medical Affairs aims to deliver clear, credible answers that distinguish us from our competitors. Our goal is to become the preferred pharmaceutical partner globally by leveraging medical expertise to provide patient-centric solutions, support healthcare providers and payers with clinical insights, and empower patients with educational resources.

Primary Responsibilities:
As a Medical Writer within our Medical Affairs team, you will play a vital role in creating and maintaining content to support various Medical Affairs activities, including:

  • Slide updates for internal training and presentations
  • Manuscript slides and data slides for publications and regulatory purposes
  • Newsletters and bulletins to disseminate important information
  • Educational materials for healthcare professionals and patients
  • Advisory board slides and competitive landscape analysis
  • Collaborating with internal and external experts to develop presentations
  • Ensuring accuracy, consistency, and compliance with regulatory guidelines in all written materials

Minimum Qualification Requirements:

  •  B Pharm / M Pharm / Bsc / Msc / Pharm D
  • Demonstrated experience in technical or regulatory scientific writing
  • Strong communication and interpersonal skills
  • Successful completion of a writing exercise as part of the evaluation process

Additional Preferences:

  • Graduate degree with a formal research component or in life sciences
  • Mastery of verbal and written English skills in medical or scientific writing
  • Experience in clinical development, clinical trials, or regulatory activities
  • Demonstrated project management and time management skills
  • Proficiency in end-user computer skills (word processing, spreadsheets, presentations)

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