Director – Medical, Clinical Research Physician

🕒 September 17

🇺🇸 United States – Remote

💵 $201k - $393.8k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

Where this job comes from

Posted on Eli Lilly and Company's careers page, not through a job board

First seen by Remote Rocketship September 17

Still open on Eli Lilly and Company's site. Checked 0 minutes ago.

Logo of Eli Lilly and Company

Eli Lilly and Company

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 and women's health therapeutic areas • Implement global clinical trials and report adverse events according to corporate patient safety requirements • Review protocols, study reports, publications, data dissemination materials, labels, grant submissions and contracts • Engage with regulatory and governmental agencies • 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 • Plan clinical studies, outcomes research and pharmacoeconomic research to address patient needs • Develop clinical strategies and plans for compounds and support Phase III planning • Design, write and oversee Phase Ib and Phase IIa/IIb clinical trials and biomarker studies • Collaborate with clinical staff, investigators, consultants, statisticians and quantitative scientists • Support PK/PD modeling, pharmacokinetic and drug metabolism studies, dosing optimization and patient population selection • Ensure study initiation and conduct comply with Good Clinical Practices, local laws and regulatory requirements • Monitor patient safety and track and follow up on adverse events • Participate in clinical data analysis, trial registry reporting, final reports, publications, presentations and congress support • Support regulatory reports, IND and Investigator Brochure medical sections, FDA advisory committee hearings, labeling modifications and risk management planning • Provide medical expertise to regulatory, health outcomes, marketing, management and business development teams • Establish relationships with external experts, thought leaders, professional societies and the medical community • Participate in patent development, trade associations, committees, initiatives and task forces • Define the Patient Journey and corresponding Moments of Truth and act as patient advocate and medical expert • Maintain expertise in relevant medical literature, clinical practice, pre-clinical and clinical data, and therapeutic-area developments • Set professional development goals, coach and provide feedback, support recruitment, diversity and retention, and lead matrixed cross-functional teams

🎯 Requirements

• Medical Doctor or Doctor of Osteopathy • Board eligible or certified in a medical specialty, or 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 communications • Board certified or eligible in Obstetrics and Gynecology, Endocrinology, or Immunology preferred • Clinical research or pharmaceutical medicine experience preferred • Knowledge of drug development process preferred • 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 to support the team

🏖️ Benefits

• Company bonus depending, in part, 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 • Disability accommodation support during the application process • Employee resource groups and support networks

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