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Senior Manager - Medical Affairs Professional - Obesity

2+ years
Not Disclosed
10 March 2, 2025
Job Description
Job Type: Full Time Education: MBBS/MD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Manager - Medical Affairs Professional (Obesity)
Location: Gurgaon, Haryana, India
Reposted: 2 days ago
Full-time | On-site

About Lilly

Lilly is a global healthcare leader dedicated to uniting caring with discovery to make life better for people around the world. Headquartered in Indianapolis, Indiana, Lilly strives to bring life-changing medicines to those in need, enhance disease understanding, and contribute to communities through philanthropy and volunteerism.

Job Summary

The Medical Affairs Professional (MAP) is a therapeutically aligned Clinical Scientist responsible for strategic and tactical thinking in lifecycle planning. This role ensures that all medical activities comply with local and international regulations, Good Clinical Practices, and company standards. The MAP collaborates cross-functionally to meet both external customer and internal business needs.

Key Responsibilities

Scientific Expertise & Medical Affairs Delivery

  • Develop and contribute to the affiliate/therapeutic area medical plan.
  • Lead/support data analysis and the development of publications (abstracts, posters, manuscripts).
  • Partner with Medical Affairs roles (CRP, CRS, MSL) for seamless customer experiences.
  • Contribute to insight generation on patient journeys, treatment patterns, and unmet needs.
  • Support CRP in preparing and executing data generation plans.
  • Create and review medical information letters.
  • Support scientific data disclosure (SDD plans).
  • Stay updated on medical and scientific developments in the therapeutic area.
  • Identify trends and projections in clinical practice and patient access.

Cross-Functional Team Collaboration

  • Serve as the key medical point of contact for cross-functional teams.
  • Provide clinical, scientific, and strategic input to support brand teams.
  • Contribute to the development of medical strategies for brand plans.
  • Review and develop promotional materials for the brand team.
  • Oversee the medical component of Patient Support Programs.
  • Support medical training needs for internal business partners.
  • Plan and implement symposia, advisory boards, and scientific exchange events.
  • Recommend Thought Leaders (TLs) and external consultants.

Customer Engagement & Experience

  • Respond to external customer questions, including escalations.
  • Drive Thought Leader engagement and speaker training.
  • Develop collaborations with professional societies.
  • Deliver scientific education via digital or in-person events.
  • Lead digital innovations for improved customer engagement.

Regulatory Collaboration

  • Support the development and review of local labeling modifications.
  • Provide medical expertise to regulatory teams.
  • Assist in regulatory report preparation and advisory committee meetings.
  • Participate in risk management planning with global and local teams.

Professional Development

  • Stay updated with training and professional development.
  • Ensure compliance with all company policies and procedures.

Key Relationships

Internal:

  • Marketing Team
  • Clinical Research Physicians
  • Regional/Global Medical Teams
  • Local Medical, Regulatory, and Clinical Teams

External:

  • Scientific Experts
  • Physicians/HCPs
  • Medical Societies

Qualifications & Experience

Educational Qualification:

  • Core: MBBS or PhD in a medically related field.
  • Desired: Doctor of Medicine (MD) in clinical or non-clinical subjects.

Knowledge & Experience:

  • Core:
    • 2+ years of industry experience in a medical/scientific role within a relevant therapeutic area.
    • Experience in customer interactions, anticipating needs, and handling non-standard requests.
    • Cross-functional collaboration experience with Marketing, GPS, Compliance, Legal, and Regulatory teams.
    • Strong business acumen.
    • Proven ability to work independently and as a team contributor.
  • Desired: 2-3 years of relevant clinical practice experience.

Skills:

  • Strong leadership and influencing ability.
  • Capacity to manage high workload and complex deliverables.
  • Ability to translate scientific data into clear, compliant content.
  • Problem-solving and analytical skills.
  • High learning agility.
  • Excellent command of English.
  • Strong communication and interpersonal skills.

Other Role Requirements:

  • Domestic and international travel may be required.
  • Field days may be required.
  • Occasional evening/weekend work.

Equal Opportunity Employer

Lilly is committed to fostering an inclusive workforce and provides accommodations for individuals with disabilities. If you require assistance with the application process, please complete the accommodation request form here.

Lilly does not discriminate based on age, race, color, religion, gender, sexual orientation, gender identity, national origin, veteran status, disability, or any other legally protected status.

 

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