Medical Director, CMH – IBU Alliance Markets
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Job Description
Medical Director guiding clinical strategy, trials, regulatory support, and scientific exchange. Supporting Lilly’s life-changing medicines across UK, Africa, Asia, and other alliance markets.
Responsibilities:
- Understand and anticipate scientific information needs of local and regional customers, including payers, patients, and health care providers
- Lead data analyses and new clinical or health outcomes research efforts to address customer questions
- Contribute to medical strategies supporting brand commercialization activities
- Collaborate with global Medical Affairs, brand, patient outcomes/real-world evidence, clinical management, and cross-functional teams on local business plans
- Comply with local laws, regulations, global policies, procedures, and compliance guidelines for data dissemination and interactions with external health care professionals
- Address unsolicited scientific information requests from external health care professionals
- Support preparation and review of medical letters and medical information materials
- Establish and maintain collaborations with external scientific experts, thought leaders, and the broader medical community
- Represent country or regional clinical needs in clinical strategy, development plans, and study protocol design
- Review and approve local informed consent documents and risk profiles
- Collaborate on the design, conduct, and reporting of local clinical trials
- Participate in development and review of local labeling and labeling modifications
- Provide medical expertise to regulatory scientists and participate in advisory committees
- Monitor clinical practice and access trends in relevant therapeutic areas
- Evaluate medical literature, competitive product data, and scientific developments
- Act as scientific consultant and protocol expert for clinical study teams and medical colleagues
Requirements:
- Medical Doctor or Doctor of Osteopathy
- Must be board eligible or certified in an appropriate specialty/subspecialty, or have completed comparable post-medical-school clinical training relevant to the country of hiring
- Must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education
- Fluent in English, both verbal and written communication
- Knowledge of the drug development process relevant to the country/region preferred
- Strong communication, organizational, and negotiation skills
- Demonstrated ability to influence others to create a positive working environment
Benefits:
- Disability accommodation support during the application process
- Equal employment opportunity and non-discrimination commitment
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