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Clinical Research Physician – Incretins

5+ years
$198,000 - $330,000
10 Jan. 28, 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

Clinical Research Physician – Incretins

Location: Indianapolis, Indiana, United States
Job Type: Full Time, Regular
Job ID: R-64932


About Lilly:

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, our employees work to bring life-changing medicines to those who need them, improve the understanding and management of diseases, and give back to our communities through philanthropy and volunteerism. We are looking for passionate individuals dedicated to improving lives.

Position Overview:

The Clinical Research Physician for the Diabetes and Obesity Business Unit – Global Medical Affairs will play a key role in supporting Lilly's incretin portfolio and patients with obesity. This role involves strategic planning for drug development and commercialization, conducting and reporting clinical trials, collaborating with various global teams, and ensuring compliance with relevant regulations. The position focuses on enhancing customer experience and supporting activities like clinical trials, regulatory affairs, pricing, reimbursement, and access, as well as scientific data dissemination.

Responsibilities:

  • Medical Affairs Support: Provide expert medical support for global and local business activities, including marketed product support and strategic planning for drug compounds.
  • Clinical Trial Design & Execution: Lead the planning, startup, and conduct of phase 3b/4 studies, with a focus on incretin therapies. Ensure successful execution of clinical trials in alignment with global strategies.
  • Collaboration & Leadership: Collaborate with cross-functional teams (clinical, regulatory, marketing) to drive business goals and scientific initiatives, including new product development and lifecycle management.
  • Regulatory & Governmental Support: Provide medical support for new drug submissions and interact with regulatory agencies to ensure compliance.
  • Scientific Communication: Lead the creation and dissemination of scientific data through presentations, publications, congresses, and meetings with key opinion leaders (KOLs) and healthcare professionals (HCPs).
  • Customer Engagement: Foster strong relationships with the healthcare community, including external scientific experts, KOLs, and relevant professional societies. Provide ongoing scientific education and support to healthcare professionals and internal teams.
  • Real-World Evidence & Patient Insights: Integrate real-world evidence, observational data, and patient-reported outcomes into clinical development programs to support commercial strategies and meet patient needs.
  • Safety Monitoring: Oversee patient safety during clinical studies and ensure proper tracking of adverse events according to corporate policies and procedures.

Qualifications:

  • Education: Medical Doctor (MD) with board eligibility or certification in Endocrinology, Diabetology, or a comparable medical specialty. Foreign medical graduates must meet local licensing requirements.
  • Experience:
    • Minimum of 5 years of clinical experience in diabetes or obesity.
    • Experience in pharmaceutical medical affairs and/or clinical development is highly preferred.
    • Strong background in drug development, clinical trial management, and regulatory compliance.
  • Skills:
    • Strong leadership, communication, and collaboration skills.
    • Ability to work cross-functionally with various teams.
    • Fluent in English, both verbal and written.
    • Demonstrated ability to balance scientific and business priorities.
  • Travel: Willingness to engage in domestic and international travel as required.

Compensation:

  • Salary Range: $198,000 - $330,000 (Actual compensation will depend on experience, education, skills, and geographic location)

Additional Information:

  • Benefits: Comprehensive benefits package, including healthcare, dental, vision, 401(k), life insurance, wellness benefits, and more.
  • Diversity & Inclusion: Lilly is committed to diversity and inclusion, ensuring equal opportunities for all applicants, including those with disabilities.

Lilly encourages individuals to actively engage in the workforce and offers strong support networks through employee resource groups (ERGs), such as the Women’s Network, Veterans Leadership Network, PRIDE (LGBTQ+ Allies), and many others.

Application Process:

For individuals requiring accommodations during the application process, Lilly provides assistance through the workplace accommodation form. Please submit your request through the provided form for any necessary adjustments.


Join us at Lilly, where we continue to make life better for people around the world.