Clinical Research Physician - Malignant Hematology
Eli Lilly and Company
August 06, 2026
Remote friendly (Indiana, United States)
United States
Clinical Research and Development
Clinical Research Physician (CRP) — Core Job Responsibilities
Clinical Planning
- Collaborate on and maintain a Draft Launch Label and Value Proposition (patient, provider, payer), product lifecycle plan, clinical strategies, development plans, and study protocol design.
- Contribute to business unit/global alignment of clinical strategy and plans.
- Stay updated on pre-clinical and clinical data relevant to the molecule.
Clinical Research/Trial Execution and Support
- Plan, review, and collaborate on clinical documents (protocols, informed consents, final reports, submissions/annual reports) to project timelines.
- Provide oversight/input into ICDs.
- Collaborate on design, conduct, and reporting of local clinical trials (sample size, patient commitment, timelines, grants, governance interactions).
- Review/approve risk profiles and ensure appropriate risk communication.
- Participate in investigator identification and selection.
- Ensure administrative study initiation/conduct requirements are completed (IRB/ethics, informed consent, regulatory approvals/notifications) per GCP and local laws.
- Support study start-up meetings and investigator/site training.
- Serve as a resource to clinical operations/monitors, investigators, and ethical review boards.
- Monitor patient safety and track/follow up adverse events per corporate patient safety.
- Review IIT proposals and publications as requested.
Scientific Data Dissemination/Exchange
- Ensure compliance with laws/policies for data dissemination and interactions with external HCPs.
- Address unsolicited scientific information needs per guidelines.
- Support clinical trial registry reporting; plan/participate in symposia and HCP meetings.
- Support medical information materials, responses to customer questions/media requests, follow-up calls/written info per SOPs.
- Support data analysis, slide sets, and publications; prepare final reports.
- Build relationships with external experts/thought leaders and professional societies.
- Support training and congress/customer events.
Regulatory Support
- Develop/review label changes/modifications with affiliates, brand, regulatory/legal.
- Provide medical expertise to regulatory scientists.
- Support regulatory reports (NDAs, FDA annual reports, PADERS), advisory committee support, local registration, and resolution of regulatory issues.
- Participate in advisory committees and risk management planning.
Business/Customer Support (pre/post launch)
- Develop medical strategies to support commercialization and local business plans.
- Lead data analyses and clinical/patient outcomes research to address payer/patient/HCP questions.
- Support payer partnership programs and defend product value within PRA.
- Provide clinical input for promotional materials/tactics; define Patient Journey and Moments of Truth.
Scientific/Technical Expertise & Development
- Critically evaluate medical literature; track competitive products and scientific developments.
- Stay current on clinical practice/access trends (near and longer term).
- Provide scientific training/consulting and act as protocol expert.
- Attend scientific symposia; pursue extramural scientific experiences.
General Responsibilities
- Support budget preparation/administration with Sr. Director-Medical.
- Set development goals; participate in recruitment, diversity, retention, coaching, and committees/task forces.
Basic Requirements
- Medical Doctor; board eligible/certified in appropriate specialty/subspecialty or comparable post-medical clinical training (US-trained physicians: board eligibility/certification required).
- Non-US trained physicians: education/training at an LCME-compliant medical school.
Additional Preferences
- 3+ years industry experience in oncology or malignant hematology.
- Demonstrated knowledge of clinical research and drug development process.
- Strong communication, interpersonal, organizational, teamwork, and negotiation skills.
Clinical Planning
- Collaborate on and maintain a Draft Launch Label and Value Proposition (patient, provider, payer), product lifecycle plan, clinical strategies, development plans, and study protocol design.
- Contribute to business unit/global alignment of clinical strategy and plans.
- Stay updated on pre-clinical and clinical data relevant to the molecule.
Clinical Research/Trial Execution and Support
- Plan, review, and collaborate on clinical documents (protocols, informed consents, final reports, submissions/annual reports) to project timelines.
- Provide oversight/input into ICDs.
- Collaborate on design, conduct, and reporting of local clinical trials (sample size, patient commitment, timelines, grants, governance interactions).
- Review/approve risk profiles and ensure appropriate risk communication.
- Participate in investigator identification and selection.
- Ensure administrative study initiation/conduct requirements are completed (IRB/ethics, informed consent, regulatory approvals/notifications) per GCP and local laws.
- Support study start-up meetings and investigator/site training.
- Serve as a resource to clinical operations/monitors, investigators, and ethical review boards.
- Monitor patient safety and track/follow up adverse events per corporate patient safety.
- Review IIT proposals and publications as requested.
Scientific Data Dissemination/Exchange
- Ensure compliance with laws/policies for data dissemination and interactions with external HCPs.
- Address unsolicited scientific information needs per guidelines.
- Support clinical trial registry reporting; plan/participate in symposia and HCP meetings.
- Support medical information materials, responses to customer questions/media requests, follow-up calls/written info per SOPs.
- Support data analysis, slide sets, and publications; prepare final reports.
- Build relationships with external experts/thought leaders and professional societies.
- Support training and congress/customer events.
Regulatory Support
- Develop/review label changes/modifications with affiliates, brand, regulatory/legal.
- Provide medical expertise to regulatory scientists.
- Support regulatory reports (NDAs, FDA annual reports, PADERS), advisory committee support, local registration, and resolution of regulatory issues.
- Participate in advisory committees and risk management planning.
Business/Customer Support (pre/post launch)
- Develop medical strategies to support commercialization and local business plans.
- Lead data analyses and clinical/patient outcomes research to address payer/patient/HCP questions.
- Support payer partnership programs and defend product value within PRA.
- Provide clinical input for promotional materials/tactics; define Patient Journey and Moments of Truth.
Scientific/Technical Expertise & Development
- Critically evaluate medical literature; track competitive products and scientific developments.
- Stay current on clinical practice/access trends (near and longer term).
- Provide scientific training/consulting and act as protocol expert.
- Attend scientific symposia; pursue extramural scientific experiences.
General Responsibilities
- Support budget preparation/administration with Sr. Director-Medical.
- Set development goals; participate in recruitment, diversity, retention, coaching, and committees/task forces.
Basic Requirements
- Medical Doctor; board eligible/certified in appropriate specialty/subspecialty or comparable post-medical clinical training (US-trained physicians: board eligibility/certification required).
- Non-US trained physicians: education/training at an LCME-compliant medical school.
Additional Preferences
- 3+ years industry experience in oncology or malignant hematology.
- Demonstrated knowledge of clinical research and drug development process.
- Strong communication, interpersonal, organizational, teamwork, and negotiation skills.