Jobs · Analyst · Indiana

Clinical Research Physician - Development, Neuroscience

Eli Lilly and Company · Indianapolis, IN · 3 wk ago
Analyst$198k–$356k/yrFull-time

About the role

The Development Clinical Research Physician (CRP) at Lilly is responsible for participating in the development, conduct, medical monitoring, and reporting of corporate/global clinical trials in support of registration and commercialization of the product. This role also involves the implementation of global clinical trials, adverse event reporting, protocol and publication review, and various medical activities in support of demand realization.

Responsibilities

  • Oversee patient safety during the conduct of studies and track and follow up on adverse events.
  • Collaborate with business unit geographical regions, Discovery, Program Phase Medicine, and Clinical Pharmacology in developing and maintaining a Draft Launch Label and Value Proposition addressing key customer needs.
  • Contribute to business unit and global alignment of clinical strategy and clinical plans.
  • Understand and stay updated with pre-clinical and clinical data relevant to the molecule.
  • Plan, collaborate on, and review scientific content of clinical documents such as protocols, informed consent documents, final study reports, and submissions.
  • Provide oversight and input into Investigator Diagnostics (ICDs).
  • Requirements

    Psychiatrist - Medical Doctor or Doctor of Osteopathy. Must be board eligible or certified in psychiatry or have completed the comparable level of post-medical school clinical training relevant to the country of hiring. US trained physicians must have achieved board eligibility or certification. Physicians trained outside the US who are not US board eligible or certified may be hired directly for employment in the US at the discretion of the Chief Medical Officer. Non-US trained physicians must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education (LCME).

    Minimum of 3 years of clinical development experience in an industry setting (or equivalent), including experience with medical monitoring.

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