Medical Director Neurology Oncology -Ibu Alliance Markets H/F Lilly

Overall Job Purpose

As a Clinical Research Physician (CRP), you will be the therapeutically aligned scientist playing a key role within the Medical Affairs organization. The primary focus of the CRP is to use knowledge of neuroscience - with a focus on dementia, and oncology experience considered a plus - available treatments, and investigational compounds to deliver strategic and tactical medical planning. The CRP partners cross-functionally, presenting at meetings with government regulatory agencies, providing medical guidance on pricing, reimbursement and access (PRA), and leading local scientific data dissemination - including presenting at conferences and advisory boards, and overseeing the scientific content of educational programs.

Key Responsibilities

Business/Customer Support

• Understand and anticipate the scientific information needs of local/regional customers (payers, patients, healthcare providers)
• Contribute to medical strategies supporting brand commercialization, working with global Medical Affairs, brand teams, Global Patient Outcomes/Real World Evidence, PRA, and clinical teams during local business plan development
• Provide clinical input to PRA activities, including payer partnership programs and product value defense
• Support business-to-business and business-to-government activities as medical expert
• Contribute to strategic planning for marketed brands
• Contribute scientific and creative input to the development and approval of promotional materials
• Support training of sales representatives and medical personnel
• Apply knowledge of market archetypes and customer insights to all customer-related activities

Scientific Data Dissemination/Exchange

• Establish and maintain relationships with external scientific experts, thought leaders, and the medical community locally, nationally, and internationally
• Serve as the scientific expert on Lilly's neuroscience (and oncology, where relevant) compounds, sharing knowledge across internal teams
• Support medical information associates in preparing and reviewing medical letters and materials
• Ensure compliance with local laws, global policies, and guidelines on data dissemination and HCP interactions
• Address unsolicited scientific information needs from external HCPs per compliance guidelines
• Support planning of speaker training, advisory boards, and other HCP meetings
• Prepare or review scientific information in response to customer or media questions, with timely follow-up per global SOPs
• Support data analysis, slide set development, and publications (abstracts, posters, manuscripts)
• Maintain relationships with relevant professional societies
• Support customer research design as medical expert
• Provide congress support (exhibits, presentations, medical booth staffing, thought leader engagement)
• Participate in Clinical Trial Registry reporting activities

Clinical Planning & Trial Execution/Support

• Represent country/region clinical needs to business unit medical leadership in developing clinical strategies, development plans, and protocol design
• Review and approve local informed consent documents and risk profiles
• Collaborate with clinical research staff on local trial design, conduct, and reporting (sample size, timelines, grants, governance)
• Review IIT proposals and publications as requested
• Contribute to global alignment of Phase 3b/4 studies (and Phase I/II where applicable)
• Address the scientific information needs of investigators and study personnel

Regulatory Support

• Participate in development and review of local labelling, in collaboration with global Development, brand, regulatory, and legal teams
• Provide medical expertise to regulatory scientists and advisory committees

Scientific Technical Expertise

• Stay current on clinical practice and access trends in neuroscience (and oncology), near-term (1-2 years) and longer-term (3-5 years)
• Critically evaluate relevant medical literature and competitive product data
• Act as scientific consultant and protocol expert for clinical study teams

Qualifications

• Medical Doctor or Doctor of Osteopathy / MBChB/MBBS with national-council registration
• Board-eligible or certified in a specialty relevant to neuroscience or oncology, or equivalent post-medical school clinical training relevant to the country of hiring
• Medical education completed at a school listed in the World Directory of Medical Schools (or equivalent)
• 5+ years' experience in Medical Affairs
• Clinical and/or research experience in neuroscience, with a focus on dementia, required; oncology experience a plus
• Fluent in English (verbal and written) required; fluent Spanish a strong plus; additional regional languages an advantage
• Knowledge of drug development process relevant to country/region preferred
• Strong communication, organizational, and negotiation skills
• Demonstrated ability to influence others and foster a positive working environment

Key Job Requirements

• Previous TA leadership across geographies
• Able to lead and provide clear direction to internal and external teams
• Strong planning, execution, and people management skills
• Comfortable interpreting technical/scientific data and communicating with credibility; good presentation skills
• Able to effectively manage medical budget
• Strong track record of teamwork in a cross-functional environment
• Willingness to travel to customers, meetings, and congresses within the Alliances and internationally (30%+ travel may be required)

Working Arrangement

Open to candidates in EMEA locations aligned with Alliances operating hours. Hybrid working may be possible depending on location and local arrangements.

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