Director – Medical, Clinical Research Physician

🔥 1 minute ago

🇺🇸 United States – Remote

💵 $201k - $393.8k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

👻 Ghost score 0%

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Eli Lilly and Company

WebsiteLinkedInAll Job Openings

10,000+ employees

💊 Pharmaceuticals

🏥 Healthcare

🧬 Biotechnology

💰 $6.5M Post-IPO Debt - Eli Lilly on 2024-02

Pharmaceuticals • Healthcare • Biotechnology

Eli Lilly and Company is a multinational pharmaceutical company that researches, develops, manufactures, and markets prescription medicines across multiple therapeutic areas including diabetes, oncology, immunology, neuroscience, and pain. Headquartered in Indianapolis, Indiana, Lilly is known for its extensive R&D, clinical development, and global commercialization of biologic and small-molecule drugs. The company focuses on drug discovery, clinical trials, regulatory approvals, and large-scale pharmaceutical manufacturing and distribution.

📋 Description

• Participate in development, conduct and reporting of global clinical trials for compounds in the cardiometabolic research therapeutic area, including women’s health • Support implementation of global clinical trials and report adverse events according to corporate patient-safety requirements • Review protocols, study reports, publications, data dissemination, labels, grant submissions, contracts, and regulatory interactions • Assess licensing opportunities and conduct outreach to external clinical customers • Work with research scientists to identify lead compounds and clinical candidates and plan pre-clinical studies • Provide internal training, peer review of clinical protocols and reports, and ad hoc scientific consultation • Work with late-stage development colleagues to plan clinical studies, outcomes research, and pharmacoeconomic research • Contribute to clinical development strategy and plans for early-phase compounds • Collaborate on design, conduct and reporting of Phase Ib and IIa/IIb trials • Integrate clinical studies with PK/PD, statistics, molecular epidemiology, ADME, modeling and simulation approaches • Design and write clinical trial protocols and oversee study implementation • Collaborate with investigators, consultants, clinical research staff, statisticians and health outcomes researchers • Monitor patient safety and track and follow up adverse events • Support clinical trial data analysis, reporting, publications, presentations, symposia and advisory boards • Support regulatory reports, IND and Investigator Brochure medical sections, FDA advisory committee hearings, labeling modifications and risk management planning • Provide medical expertise to regulatory scientists and business units • Advise on potential markets for development and licensed compounds and support business development • Build relationships with external experts, thought leaders, professional societies and the medical community • Participate in patent development and define the Patient Journey and Moments of Truth • Maintain current knowledge of medical literature, clinical practice, pre-clinical and clinical data, and therapeutic-area developments • Set professional development goals, coach colleagues, participate in recruitment and retention efforts, and lead matrixed cross-functional teams

🎯 Requirements

• Medical Doctor or Doctor of Osteopathy • Must be board eligible or certified in a medical specialty, or have completed comparable post-medical-school clinical training relevant to the country of hiring • U.S.-trained physicians must have achieved board eligibility or certification • Non-US-trained physicians must have completed education and training at a medical school meeting LCME requirements • Fluent in English, both written and verbal • Interpersonal, organizational and negotiation skills • Ability to influence others cross-functionally and within the function • Excellent teamwork skills • Willingness to engage in domestic and international travel as appropriate • Board certified or eligible in Obstetrics and Gynecology preferred • Clinical research or pharmaceutical medicine experience preferred • Knowledge of drug development process preferred

🏖️ Benefits

• Company bonus depending partly on company and individual performance • Company-sponsored 401(k) • Pension • Vacation benefits • Medical, dental, vision and prescription drug benefits • Flexible benefits, including healthcare and/or dependent day care flexible spending accounts • Life insurance and death benefits • Time off and leave of absence benefits • Well-being benefits, including employee assistance program, fitness benefits, and employee clubs and activities • Employee resource groups offering support networks • Disability accommodation support during the application process