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Alliance Diabetes & Obesity Crp

5+ years
Not Disclosed
10 Feb. 25, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Job Title: Alliance Diabetes & Obesity CRP

Location: GURGAON, Haryana, India
Category: Medical
Job Type: Full Time Regular
Job ID: R-59040


About Eli Lilly:

Eli Lilly is a global healthcare leader, headquartered in Indianapolis, Indiana. Their mission is to make life better for people worldwide by discovering and bringing life-changing medicines to those in need, improving disease understanding and management, and giving back to communities.


Role Overview:

The Alliance Diabetes & Obesity CRP is responsible for supporting medical affairs activities related to diabetes and obesity. The position focuses on developing and disseminating scientific information, contributing to clinical research, and supporting regulatory processes while collaborating with cross-functional teams.


Key Responsibilities:

  1. Business/Customer Support:

    • Address scientific information needs of local/regional customers.

    • Lead data analyses and clinical research efforts to support brand commercialization.

    • Contribute to local business plan development and medical strategy.

  2. Scientific Data Dissemination/Exchange:

    • Ensure compliance with laws and regulations concerning data dissemination and interactions with healthcare professionals.

    • Support medical information associates in preparing materials.

    • Build relationships with external scientific experts and thought leaders.

  3. Clinical Planning & Research Support:

    • Represent local clinical needs in business unit medical leadership.

    • Assist with the design and reporting of local clinical trials.

    • Review and approve local consent documents and risk profiles.

  4. Regulatory Support:

    • Collaborate in developing and reviewing local labelling.

    • Provide medical expertise to regulatory teams.

    • Participate in advisory committees.

  5. Scientific Technical Expertise:

    • Stay updated on trends and projections in clinical practice.

    • Critically evaluate medical literature and competitive product data.

    • Serve as a scientific consultant and protocol expert for clinical study teams.


Qualifications & Experience:

  • Required:

    • Medical Doctor or Doctor of Osteopathy.

    • Board eligible/certified in the appropriate specialty/subspecialty or relevant post-medical school training.

    • Fluent in English (verbal and written).

    • Strong communication, organizational, and negotiation skills.

  • Preferred:

    • Knowledge of drug development processes.

    • Ability to influence and create positive working environments.


Equal Opportunity Employer:

Eli Lilly is committed to ensuring equal opportunities for all applicants, including those requiring accommodations. If you need an accommodation to submit a resume, you can complete the accommodation request form for further assistance.


How to Apply:
For more details or to apply, visit
Eli Lilly Careers.

#WeAreLilly