Medical Affairs Internship By Eli Lilly India
Medical Affairs Internship By Eli Lilly India
Lilly is a global healthcare leader dedicated to discovering and delivering life-changing medicines. The Medical Affairs (MA) internship focuses on providing accurate, balanced, and timely scientific information to healthcare professionals, regulators, payers, and patients. Interns will support the development of medical content such as slides, newsletters, patient and HCP education materials, and competitive landscape documents. The role combines scientific research, medical writing, and collaboration with cross-functional teams to ensure the delivery of high-quality, evidence-based information across the product lifecycle.
Documents Required
Applicants submit the following documents:
  • Resume/CV
  • Valid Email ID
  • Mobile No.
  • Study Mark Sheets
  • Certificates (If you have)
  • Cover letter (If applicable)
  • Eligibility Criteria
    Applicants must meet the following criteria:
  • Master’s degree in a scientific, health, communications, or technology-related health field.
  • Strong written and verbal communication skills in English.
  • Knowledge or experience in clinical pharmacology, therapeutic areas, or medical writing is preferred.
  • Demonstrated ability to manage projects and meet deadlines.
  • Experience with regulatory, clinical trial, or Medical Affairs documents is a plus.
    Additional Preferences:
  • Advanced degree or certification in life sciences, pharma, epidemiology, pharmacoeconomics, or related disciplines.
  • Expertise in specific therapeutic areas such as neuroscience, oncology, cardiovascular, immunology, or endocrine disorders.
  • Familiarity with document management systems and scientific communications tools.
    Note: This internship is exclusively available in India. Specifically, in Bengalore.
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    Responsibilities
    Interns will:
  • Develop and maintain high-quality medical affairs deliverables including slide decks, newsletters, and educational materials.
  • Collect, evaluate, and synthesize data from multiple sources to create cohesive content strategies.
  • Plan, draft, review, edit, and finalize documents while ensuring scientific accuracy and consistency.
  • Coordinate with internal teams, external experts, and vendors to gather input and manage quality checks.
  • Support project management by tracking timelines, identifying risks, and communicating progress.
  • Maintain and enhance knowledge of therapeutic areas, compounds, and regulatory/publication guidelines.
  • Contribute to process improvements and share best practices across teams.
  • How To Apply
    Follow the below steps to apply for the program:
    1. Visit Our Official Website.
    2. Read carefully all the information about the program details.
    3. Click on the "Register" to complete the registration with required details.
    4. After successful registration, Use the received credentials to log into your account.
    5. Once logged in, Click on the "Apply" button.
    6. You will be directed to the application form. Fill in all the required details accurately.
    7. Prepare the necessary documents as specified in the application requirements.
    8. Upload these documents in the designated sections of the application form.
    9. Before submitting, review all the information you have provided.
    10. After that, Click on the "Submit” button to submit your application.
    Note: "As a free user,"
    →'You're encouraged to share this valuable information with your friends to access the link properly'.

    Stipend

    Medical Affairs Internship By Eli Lilly India
    SCHOLARSHIP PROVIDER
    Eli Lilly India
    APPLICATION DEADLINE
    09 November
    EDUCATION LEVEL
    Masters
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    Lilly is a global healthcare leader dedicated to discovering and delivering life-changing medicines. The Medical Affairs (MA) internship focuses on providing accurate, balanced, and timely scientific information to healthcare professionals, regulators, payers, and patients. Interns will support the development of medical content such as slides, newsletters, patient and HCP education materials, and competitive landscape documents. The role combines scientific research, medical writing, and collaboration with cross-functional teams to ensure the delivery of high-quality, evidence-based information across the product lifecycle.