Sr. Director Medical Oral Therapies

Eli Lilly And Company; Xico; Presencial; MXN 2,733,000 - 3,645,000; Jornada completa

Descripción de la vacante

A global healthcare leader is looking for a Sr. Director Medical Oral Therapies in Xico, Mexico. This full-time role involves providing expert medical support, collaborating on clinical trials, and leading medical affairs activities. Candidates should have an MD or equivalent, at least 5 years of experience, and strong communication skills. Immediate start availability is preferred. The position offers an opportunity to influence the business and enhance the customer experience in a dynamic environment.

Formación

• At least 5 years of experience in the therapeutic area.
• Ability to influence cross-functionally.
• Fluent in English (verbal and written).

Responsabilidades

• Provide expert medical support to enhance customer experience.
• Support product development and regulatory affairs.
• Collaborate with global teams on clinical trials.
• Lead medical affairs activities and train peers.

Conocimientos

Deep product knowledge

Strong communication skills

Interpersonal skills

Teamwork

Negotiation skills

Educación

Medical Doctor

Endocrinologist or MSc / PhD

Descripción del empleo

Join to apply for the Sr.

Director Medical Oral Therapies role at Eli Lilly and Company.

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.

Role Summary

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 CRP's specific activities include developing or contributing to the medical plan in the designated therapeutic area, supporting the conduct of local clinical trials, reporting adverse events, reviewing protocols and study reports, managing new and updated labels, documenting product pricing and reimbursement, engaging with regulatory agencies, and leading outreach medical activities to the external clinical community and thought leaders.

Primary Responsibilities

Provide expert medical support to all aspects of the local business, enhancing the customer experience.

Support product development, regulatory affairs, pricing, reimbursement and access, and scientific data dissemination.

Collaborate with global teams in planning, startup and conduct of phase 3b / 4 studies and other clinical trials.

Serve as a single point of contact for the overall molecule medical affairs.

Lead pre-, peri- and post-launch medical affairs activities and train affiliate peers.

Key Responsibilities

• Leverage deep product knowledge and educate local affiliate peers for launch readiness.
• Collaborate with International Therapeutic Area Lead and Marketing teams to ensure robust brand planning.
• Balance scientific priorities with business priorities.
• Demonstrate strong communication, interpersonal, teamwork, organization and negotiation skills.
• Influence others across functions to create a positive working environment.
• Travel domestically and internationally as required to support the business.
• Fluent in English (verbal and written).

Qualifications

• Medical Doctor.
• Endocrinologist or MSc / PhD with at least 5 years of experience in the therapeutic area.
• Demonstrated ability to influence cross-functionally and within the function.
• Ability to engage in domestic and international travel appropriate to the role.
• Fluent in English.

Other Information

Primary internal interactions: Therapeutic area directors, product directors, clinical research staff, scientific communication associates, medical information associates, global patient outcomes research consultants, regulators, legal counsel, therapeutic area physicians, and corporate patient safety physicians.

External contacts: Scientific and clinical experts, thought leaders, Lilly investigators, regulatory agency personnel, professional association staff, disease advocates, formulary representatives.

The selected candidate should have immediate start availability.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities.

Seniority Level: Director | Employment Type: Full-time | Job Function: Other (Pharmaceutical Manufacturing)

If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form. 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.