Medical Director, Genetic Medicines

🔥 14 hours ago

🍂 Massachusetts – Remote

🍂 Massachusetts – Remote

💵 $217.5k - $389.4k / 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

• Contribute to global clinical strategy and clinical plans in collaboration with Discovery • Keep updated on preclinical and clinical data relevant to molecules • Plan, collaborate on, and review protocols, informed consent documents, final study reports, and regulatory submissions • Provide oversight and input into clinical development plans • Collaborate on the design, conduct, and reporting of local clinical trials • Review and approve study risk profiles and ensure appropriate risk communication • Participate in investigator identification and selection • Ensure study initiation and conduct requirements comply with GCP and local laws • Participate in study start-up meetings and train investigators and site personnel • Serve as a resource to clinical operations personnel, monitors, investigators, and ethics boards • Monitor patient safety and track and follow up on adverse events • Support scientific data dissemination, including registries, symposia, advisory boards, presentations, analyses, and publications • Establish relationships with external experts, thought leaders, healthcare professionals, and the medical community • Support training of medical personnel and provide congress support • Participate in label changes, regulatory reports, FDA advisory committee preparation, registration efforts, and regulatory issue resolution • Participate in advisory committees and risk management planning • Contribute medical expertise to commercialization, payer partnership, product value, business-to-business, and business-to-government activities • Support promotional material development and approval • Define the Patient Journey and act as patient advocate and medical expert • Evaluate medical literature, competitive products, clinical practice trends, and access projections • Serve as scientific consultant and protocol expert • Set professional development goals, support budgets, recruitment, diversity, retention, coaching, training, and partner collaboration • Model leadership behaviors and represent patients and the Lilly brand

🎯 Requirements

• Medical Doctor or Doctor of Osteopathy • Must be board eligible or certified in a relevant field, 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 • Non-US trained physicians must have completed education and training at a medical school meeting LCME requirements • Experience in gene therapy and/or rare disease Medical Affairs or Patient Advocacy • Minimum of 3-5 years of experience in clinical research within the pharmaceutical industry or academic research setting • Understanding of drug development processes, Good Clinical Practice (GCP), and regulatory requirements • Experience with global clinical trials is a plus • Strong scientific acumen and ability to critically evaluate clinical data • Ability to comprehend and communicate complex scientific content clearly and concisely • Advanced presentation and computer skills with expertise in literature identification • Demonstrated leadership skills and ability to balance scientific and business priorities • Ability to manage multiple priorities and projects • Strong communication, interpersonal, teamwork, organizational, and negotiation skills • Ability to build professional relationships and networks • Ability to influence others cross-functionally and within the function • Ability to work effectively in a multidisciplinary team environment • Ability to travel domestically and internationally as appropriate • Fluent in English, verbally and in writing

🏖️ Benefits

• Company bonus depending on company and individual performance • Company-sponsored 401(k) • Pension • Vacation benefits • Medical benefits • Dental benefits • Vision benefits • 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 (ERGs)