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    Clinical Research Physician (Ta Lead) - Neuroscience

    Lilly
    2+ years
    Not Disclosed
    Gurgaon
    10 Jan. 16, 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: Clinical Research Physician (Therapy Lead) – Neuroscience
    Location: [Location]
    Minimal Travel Expected

    At Lilly, we unite caring with discovery to improve lives globally. As a leading healthcare company headquartered in Indianapolis, Indiana, we are committed to discovering life-changing medicines and improving the understanding and management of diseases. Our teams work to bring medicines to patients, give back to communities, and make life better for people around the world. We’re looking for determined individuals who share our vision and values.

    Purpose of the Role:

    The Clinical Research Physician (CRP) – Neuroscience plays a key role in driving medical strategies and scientific expertise for Lilly's Neuroscience portfolio, which includes conditions such as Alzheimer's Disease and Dementia. The CRP works closely with medical affairs, clinical development, and business unit teams to support product commercialization, enhance the customer experience, and ensure patients’ needs are met. The role involves collaborating with global teams, contributing to the development and execution of clinical plans, managing clinical trials, and providing leadership in the medical space.

    Key Responsibilities:

    1. Provide Medical Expertise in Neuroscience:

    • Offer scientific and medical input into the development and execution of clinical and commercialization strategies for Alzheimer’s Disease, Dementia, and other neuroscience conditions.
    • Stay current with relevant data on molecules, clinical trials, and competitor products.
    • Partner with internal teams such as Clinical Operations, Marketing, and Global Product Safety to ensure the scientific and clinical strategy aligns with business goals.

    2. Strategic Leadership and Collaboration:

    • Develop and maintain relationships with key stakeholders, including clinicians, thought leaders, and external groups.
    • Lead and contribute to medical education activities and provide scientific input for promotional materials.
    • Provide training and mentorship to other medical staff such as Medical Affairs Professionals (MAPs) and Medical Science Liaisons (MSLs).
    • Engage in the development of payer partnership programs and defend product value in collaboration with the Pricing, Reimbursement & Access (PRA) teams.

    3. Clinical Planning, Research, and Execution:

    • Drive the clinical trial planning process, ensuring successful execution of both global and regional clinical trials in line with quality, speed, and value.
    • Participate in investigator selection, trial start-up, site management, and the resolution of clinical trial issues.
    • Contribute to regulatory submissions, Health Technology Assessments (HTAs), and other regulatory requirements as needed.

    4. Scientific Data Dissemination & Compliance:

    • Provide ongoing analysis and interpretation of clinical data to support internal and external communication.
    • Ensure all medical activities comply with local and international laws and regulations (e.g., GCP, FDA, ICH).
    • Support symposia, advisory boards, and medical meetings, ensuring compliance with industry standards and Lilly policies.

    5. External Relations:

    • Establish and maintain relationships with external HCPs, advocacy groups, and other healthcare professionals to facilitate product knowledge and support clinical development.
    • Share relevant product data and clinical trial findings with HCPs and ensure their involvement in key scientific discussions and publications.

    6. People Responsibilities:

    • Mentor and guide direct reports (if applicable) such as MAPs, supporting their performance and career development.
    • Collaborate with MSL teams to enhance their scientific knowledge on the disease area and clinical trial data.
    • Participate in recruitment, retention, and diversity efforts for the medical team.

    Qualifications:

    Basic Requirements:

    • Basic Medical Qualification (MBBS/MD) and full Medical Council registration or eligibility.
    • Experience in clinical and/or industry expertise within the Neuroscience domain, particularly in Alzheimer’s Disease and Dementia (highly desirable).
    • Strong teamwork, interpersonal, and communication skills.
    • Demonstrated ability to balance scientific and business priorities.
    • Leadership capabilities with a strong track record of developing new opportunities and driving strategic initiatives.
    • Ability to manage time effectively and prioritize tasks in a fast-paced environment.
    • Fluency in English, both verbal and written.

    Additional Preferences:

    • Experience in clinical trial design and execution.
    • Awareness of the role of medical doctors in a commercial setting.
    • Ability to travel both domestically and internationally as required.

    Lilly Commitment to Equal Opportunity:

    Lilly is dedicated to providing equal opportunities for individuals with disabilities to engage in the workforce. If you require accommodation during the application process, please complete the accommodation request form here.

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

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