Clinical Research Physician - Oncology
Eli Lilly and Company
June 26, 2026
Remote
United States
Clinical Research and Development
Role Overview
- Design and run global clinical trials; support registration/commercialization.
- Contribute to protocol development, study reporting, data dissemination, publications, labeling updates, and documents for pricing/reimbursement/access.
- Ensure adverse event reporting and serve as a key scientific resource to study teams and product strategy.
Core Responsibilities (Development CRP; late-phase/marketed compounds)
Clinical Planning
- Collaborate to develop/maintain launch label/value proposition, product lifecycle plan, clinical strategies, development plans, and protocol design.
- Align global clinical strategy/plans; stay current on relevant pre-clinical/clinical data.
Clinical Research / Trial Execution
- Plan, review, and support clinical documents (protocols, informed consent, final reports, submissions).
- Collaborate on local trial design/conduct/reporting; review risk profiles.
- Support investigator selection; ensure initiation/admin requirements per GCP and local laws.
- Participate in start-up meetings; support study conduct questions.
- Monitor patient safety and track/follow up adverse events.
Data Dissemination / Regulatory / Customer Support
- Address unsolicited medical information needs; support publications and medical materials; participate in trial registry reporting.
- Prepare/review label changes and support regulatory reports (e.g., NDAs, FDA annual reports, PADERs) and risk management planning.
- Provide scientific/medical expertise for payer/provider needs and promotional material scientific input.
Qualifications & Requirements
- Medical Doctor; board eligible/certified in relevant specialty/subspecialty (or equivalent post-medical training for country of hiring).
- International oncology practice experience.
- LCME-compliant medical education/training for non-US trained physicians.
- Fluent English (written/verbal).
- Demonstrated knowledge of drug development process.
Preferred Skills/Experience
- In-depth breast oncology; experience with CDK4/6 inhibitors.
- Strong communication, interpersonal, organization, teamwork, negotiation; ability to influence cross-functionally.
- Clinical research/pharmaceutical medicine experience preferred.
- Ability to travel as needed (domestic/international).
- Design and run global clinical trials; support registration/commercialization.
- Contribute to protocol development, study reporting, data dissemination, publications, labeling updates, and documents for pricing/reimbursement/access.
- Ensure adverse event reporting and serve as a key scientific resource to study teams and product strategy.
Core Responsibilities (Development CRP; late-phase/marketed compounds)
Clinical Planning
- Collaborate to develop/maintain launch label/value proposition, product lifecycle plan, clinical strategies, development plans, and protocol design.
- Align global clinical strategy/plans; stay current on relevant pre-clinical/clinical data.
Clinical Research / Trial Execution
- Plan, review, and support clinical documents (protocols, informed consent, final reports, submissions).
- Collaborate on local trial design/conduct/reporting; review risk profiles.
- Support investigator selection; ensure initiation/admin requirements per GCP and local laws.
- Participate in start-up meetings; support study conduct questions.
- Monitor patient safety and track/follow up adverse events.
Data Dissemination / Regulatory / Customer Support
- Address unsolicited medical information needs; support publications and medical materials; participate in trial registry reporting.
- Prepare/review label changes and support regulatory reports (e.g., NDAs, FDA annual reports, PADERs) and risk management planning.
- Provide scientific/medical expertise for payer/provider needs and promotional material scientific input.
Qualifications & Requirements
- Medical Doctor; board eligible/certified in relevant specialty/subspecialty (or equivalent post-medical training for country of hiring).
- International oncology practice experience.
- LCME-compliant medical education/training for non-US trained physicians.
- Fluent English (written/verbal).
- Demonstrated knowledge of drug development process.
Preferred Skills/Experience
- In-depth breast oncology; experience with CDK4/6 inhibitors.
- Strong communication, interpersonal, organization, teamwork, negotiation; ability to influence cross-functionally.
- Clinical research/pharmaceutical medicine experience preferred.
- Ability to travel as needed (domestic/international).