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    Associate Vice President, Cardiometabolic Health - Incretin Outcome Trials, Clinical Research Physician

    Eli Lily
    5+ years
    $252,000 - $369,600
    Indianapolis
    10 Jan. 31, 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: Associate Vice President, Cardiometabolic Health - Incretin Outcome Trials, Clinical Research Physician
    Location: Indianapolis, Indiana, United States
    Category: Research & Development
    Job Type: Full-Time, Regular
    Job ID: R-72997

    About Eli Lilly & Co.

    At Lilly, we unite caring with discovery to make life better for people around the world. As a global healthcare leader headquartered in Indianapolis, Indiana, we are committed to discovering and delivering life-changing medicines. Our global team is driven by purpose, working together to improve disease management, bring innovative solutions to communities, and make life better for patients globally.

    Role Overview:

    The Associate Vice President (AVP) of Cardiometabolic Health - Incretin Outcome Trials will play a pivotal role in leading and overseeing the development, execution, and reporting of global clinical trials related to metabolic dysfunction-associated steatohepatitis (MASH). This critical leadership position requires a certified hepatologist with significant experience in MASH trials to support a future MASH outcome trial. The Clinical Research Physician (CRP) will provide day-to-day medical leadership for the trial and report to the AVP/Medical Director, Incretin Outcomes.

    Key Responsibilities:

    • Clinical Trial Leadership: Lead the development, conduct, and reporting of clinical trials in support of MASH products, ensuring adherence to regulatory and corporate requirements.
    • Medical Oversight: Provide day-to-day medical oversight of trial operations, working closely with the trial team to ensure adherence to protocols and timelines.
    • Regulatory and Safety Compliance: Ensure that all adverse events are reported in accordance with corporate patient safety protocols and regulatory requirements.
    • Protocol and Data Review: Review and provide input on study protocols, study reports, publications, and other documents supporting product development, labeling, and reimbursement strategies.
    • External Engagement: Engage with thought leaders and the external clinical customer community to ensure ongoing collaboration and scientific input.
    • Business Strategy: Contribute to the global strategy for the product’s lifecycle, including commercialization and post-marketing activities.
    • Leadership and Mentoring: Mentor junior clinical research staff and provide guidance on scientific and operational aspects of the trial. Act as a scientific resource across departments.
    • Global Collaboration: Work with global teams to ensure effective implementation and execution of clinical trials.

    Basic Qualifications:

    • Medical Degree: MD or equivalent medical degree, board eligibility or certification in a medical specialty relevant to clinical trial work.
    • Experience: Proven experience in metabolic dysfunction-associated steatohepatitis (MASH) clinical trials or a related area in hepatology.
    • Training: Board certification in hepatology or gastroenterology is preferred, with additional advanced degrees (e.g., PhD, MBA) being a plus.
    • Communication Skills: Fluent in English with excellent verbal and written communication abilities.
    • Leadership: Demonstrated leadership skills with the ability to influence cross-functional teams and external stakeholders effectively.
    • Travel: Ability to travel domestically and internationally (approximately 10-15%).

    Preferred Qualifications:

    • Knowledge of Obesity and MASH: Strong understanding of obesity and the drug development process for MASH therapies.
    • Experience: In-depth knowledge of clinical trial design and the molecule lifecycle in cardiometabolic health.
    • Additional Skills: Expertise in clinical research, regulatory affairs, and trial execution within a pharmaceutical environment.

    Compensation:

    • The anticipated salary range for this position is $252,000 - $369,600, dependent on education, experience, and geographic location. Additional performance-based incentives and comprehensive benefits, including health, dental, vision, retirement plans, and wellness programs, are also offered.

    Lilly Benefits:

    Lilly offers a competitive benefits package, including eligibility for company bonuses, 401(k), pension, medical, dental, and vision benefits, along with additional wellness initiatives such as fitness programs and employee support services. Benefits are tailored to enhance work-life balance and overall well-being.

    Equal Opportunity Employer:

    Lilly is an equal opportunity employer, ensuring equal opportunity for all individuals regardless of age, race, gender, sexual orientation, disability, or other legally protected status. We are committed to creating a diverse and inclusive environment.

    If you're ready to make a meaningful impact in clinical research and healthcare innovation, we encourage you to apply and join our dedicated team at Lilly!

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