Senior Director Global Medical Affairs (Cardiovascular/Cardiometabolic Health)

Eli Lilly and Company • Indianapolis, IN

99d • $198,000 - $356,400

About The Position

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Purpose: Through the application of scientific and medical training, clinical expertise, and relevant clinical experience, the Cardiovascular/Cardiometabolic Business Unit – Global Medical Affairs Clinical Research Physician (CRP) Senior/Executive Director is an integral member of the medical affairs team for strategic planning in the support of launch and commercialization activities to meet patients’ needs and ultimately enhance the customers’ experience in interacting with the company. The definition of “customer” here includes patients, providers (HCPs) and payers. The Senior/Executive Director may also work closely with global Development teams, Therapeutic Area Program Phase, Early Phase / Clinical Pharmacology, and Translational Medicine teams in new product development activities over the entire spectrum of drug development and clinical trial phases.

Requirements

• Medical Doctor or Doctor of Osteopathy.
• Board eligible or certified in appropriate specialty/subspecialty.
• Minimum 2 years of clinical experience in cardiovascular medicine.

Nice To Haves

• Cardiology board eligible or certified is strongly preferred.
• Prior pharmaceutical industry experience in medical affairs or clinical development preferred.
• Knowledge of drug development process preferred.
• Demonstrated ability to balance scientific priorities with business priorities.
• Demonstrated ability to influence others to create a positive working environment.

Responsibilities

• Provide expert medical support to all aspects of the local/global business.
• Participate in the development of the 'patient journey' and the strategic plan for the compound.
• Provide medical support for regulatory affairs and interactions with government agencies.
• Lead in scientific data dissemination, including leading and presenting at conferences and advisory boards.
• Plan, startup, and conduct phase 3b/4 studies.
• Support the planning of symposia, advisory board meetings, and other meetings with health care professionals.
• Prepare or review scientific information in response to customer questions or media requests.
• Establish and maintain collaborations with external scientific experts and thought leaders.
• Monitor patient safety during the conduct of studies and track adverse events.
• Collaborate with Clinical Research Scientists and clinical operations staff in protocol development.

Benefits

• 401(k) plan
• Pension
• Vacation benefits
• Medical, dental, vision, and prescription drug benefits
• Flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
• Life insurance and death benefits
• Employee assistance program
• Fitness benefits
• Employee clubs and activities

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: No Education Listed
• Number of Employees: 5,001-10,000 employees