Sr. Director Medical Affairs Neuro

hace 3 semanas

distrito federal, México Lilly A tiempo completo

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.

Clinical Research Physician (CRP)* - Medical Affairs

Purpose:

Through the application of scientific and medical training, clinical expertise, and relevant clinical experience, the Business Unit- Medical Affairs Clinical Research Physician (CRP) is an integral member of the medical affairs, development or a business unit brand 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 CRP 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.

Primary Responsibilities:

  • Provide expert medical support to all aspects of the local business, to ultimately enhance the customers' experience in interacting with the company.
  • Support local marketed product development and commercialization activities.
  • Medical support for regulatory affairs and interactions with government agencies.
  • Lead local scientific data dissemination and present at conferences, advisory boards, etc.
  • Participate in local or national trade associations, as appropriate.
  • Monitor patient safety during the conduct of studies and conduct the appropriate tracking and follow-up of adverse events.

Minimum Qualifications:

  • Medical Doctor. Must be board eligible or certified in appropriate specialty/subspecialty or have completed the comparable level of 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 (LCME).
  • Demonstrated strong communication, interpersonal, teamwork, leadership, organizational and negotiation skills.
  • Ability to engage in domestic and international travel to the degree appropriate to support the business of the team.
  • Fluent in English, verbal and written communication.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( for further assistance.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

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