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    Alliance Diabetes & Obesity Crp

    Eli Lily
    0-2 years
    Not Disclosed
    Bengaluru Chennai Hyderabad
    10 Jan. 29, 2025
    Job Description
    Job Type: Full Time Education: B.Sc, M.Sc, B.Pharm, M.Pharm, LifeScience Graduates 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: Multiple Locations (6 locations available)
    Category: Medical
    Job Type: Full-Time, Regular
    Job ID: R-59040

    Company Overview:

    At Lilly, we unite caring with discovery to improve lives worldwide. As a global healthcare leader, we are committed to bringing life-changing medicines to those in need, advancing disease understanding and management, and making a difference through philanthropy and volunteerism. We are dedicated to doing our best and putting people first. We seek individuals who are determined to make a positive impact on global healthcare.

    Job Purpose:

    The Alliance Diabetes & Obesity CRP is responsible for supporting medical and scientific strategies related to the Diabetes and Obesity therapeutic areas. This role will involve working closely with global and local teams to deliver scientific data, engage with external healthcare professionals, contribute to clinical research, and provide regulatory support.

    Key Responsibilities:

    Business/Customer Support:

    • Understand and anticipate the scientific information needs of local/regional stakeholders, including payers, patients, and healthcare providers.
    • Lead data analyses and clinical or health outcomes research to address scientific questions and needs.
    • Collaborate with global Medical Affairs, brand teams, and cross-functional stakeholders in the development of local business plans and medical strategies to support brand commercialization activities.

    Scientific Data Dissemination & Exchange:

    • Ensure compliance with local regulations and global policies regarding data dissemination and healthcare professional interactions.
    • Address unsolicited scientific information needs of healthcare professionals, adhering to compliance guidelines.
    • Support medical information associates in the preparation and review of medical letters and other information materials.
    • Build and maintain relationships with external scientific experts, thought leaders, and the broader medical community on local, national, and possibly international levels.

    Clinical Planning & Trial Execution:

    • Represent the country/region’s clinical needs to business unit medical leadership in clinical strategy and development plan discussions.
    • Assist in the design and execution of clinical trials, including review of informed consent documents, risk profiles, patient recruitment, and governance.
    • Collaborate with clinical research teams to ensure timely and efficient study execution, including sample size determination, patient commitment, and adherence to timelines.

    Regulatory Support Activities:

    • Participate in the development and review of local labeling and modifications in collaboration with global teams, regulatory affairs, and legal departments.
    • Provide medical expertise to regulatory scientists and contribute to advisory committee activities.

    Scientific Technical Expertise:

    • Stay up-to-date with trends, projections, and current clinical practices within the Diabetes and Obesity therapeutic areas.
    • Critically evaluate relevant medical literature, competitive product data, and medical developments.
    • Serve as a scientific consultant and protocol expert for clinical study teams.

    Required Qualifications:

    • Medical Doctor (MD) or Doctor of Osteopathy (DO). Board eligibility or certification in an appropriate specialty/subspecialty is required, or completion of equivalent post-medical school clinical training relevant to the country of hire.
    • Medical education and training from a medical school accredited by the Liaison Committee on Medical Education (LCME).
    • Fluent in English, with strong verbal and written communication skills.
    • Knowledge of the drug development process, particularly as it pertains to the country/region of employment.
    • Demonstrated ability to influence and build strong relationships within cross-functional teams.
    • Strong organizational, communication, and negotiation skills.

    Preferred Skills:

    • Previous experience in clinical research, regulatory affairs, or medical affairs within the Diabetes and Obesity therapeutic areas.
    • Familiarity with local and international medical regulations and compliance guidelines.
    • Experience in data analysis, scientific communication, and managing stakeholder relationships.

    Additional Information:

    Lilly is committed to providing equal opportunities to individuals with disabilities. If you need accommodation to submit your resume or application, please complete the accommodation request form here. This is for individuals who require accommodation as part of the application process, and other inquiries will not receive a response.

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