Sr. Director Medical Affairs Alzheimer

hace 2 meses

Bogotá, Colombia Eli Lilly and Company 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. Specific activities include developing or contributing to the global and/or regional clinical/medical plan in his/her therapeutic area of responsibility, the development, conduct and reporting of local clinical trials; the reporting of adverse events as mandated by corporate patient safety; review process for protocols, study reports, publications and data dissemination for products; new and updated labels, documents and tools supporting product pricing, reimbursement, and access (PRA), grant submissions and contracts; contacts with regulatory and other governmental agencies; the outreach medical activities aimed at the external clinical customer community, including thought leaders; and various medical activities in support of demand realization. In addition, with input from the Director-Medical and Business Unit Team Physician/Regional Medical Leader, the CRP is responsible for assuring that his/her activities are clearly aligned with the strategic priorities of the respective business unit global Medical Affairs team, brand team(s), global Development team, Therapeutic Area Program Phase, Early Phase/ Clinical Pharmacology, and Translational Medicine team(s).

Primary Responsibilities:

  • The primary responsibility of the Business Unit - Medical Affairs CRP is to provide expert medical support to all aspects of the local business, to ultimately enhance the customers' experience in interacting with the company. This includes local marketed product support (participate in the development of the "patient journey", knowledge journey, segmentation, unmet need analysis for the elaboration of a comprehensive annual medical plan reflective of such analysis and in alignment with product strategy.
  • The CRP is responsible for proposing and conducting Scientific activities that anchor the unmet needs of the medical scientific community and the strategic plan for the compound, medical support for regulatory affairs and interactions with government agencies, medical support for pricing, reimbursement and access (PRA), and leading in local scientific data dissemination.

Minimum Qualification Requirements:

  • 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).
  • Knowledge of drug development process relevant to country/region preferred.
  • Demonstrated ability to balance scientific priorities with business priorities.
  • Demonstrated strong communication, interpersonal, teamwork, leadership, organizational and negotiation skills.
  • Demonstrated drive and learning agility.
  • Demonstrated ability to influence others (both cross-functionally and within the function) in order to create a positive working environment.
  • 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.

Other Information:

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. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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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