Manager, Program Excellence – (IS, MRC)

Novartis Farmacéutica; Victoria de Durango; Presencial; MXN 700,000 - 1,000,000; Jornada completa

Descripción de la vacante

Una firma farmacéutica busca un Manager de Program Excellence para supervisar el manejo y ejecución de ensayos clínicos, promoviendo la colaboración interfuncional y la innovación en procesos. El candidato ideal cuenta con experiencia en gestión de proyectos y habilidades de inglés avanzado. Se espera que el rol contribuya significativamente a la eficiencia de las operaciones clínicos en el departamento.

Formación

• Mínimo 5 años de experiencia en gestión de proyectos, con 3 en ejecución de ensayos clínicos.
• Capacidad probada para trabajar de forma independiente y en equipos, apoyando múltiples proyectos.
• Experiencia en reuniones críticas con partes interesadas interfuncionales.

Responsabilidades

• Gestionar y ejecutar revisiones médicas de conceptos, planes de proyectos y protocolos.
• Colaborar con equipos clínicos e IT para resolver problemas y proporcionar informes rápidos.
• Implementar soluciones innovadoras para acelerar las actividades de generación de datos.

Conocimientos

Gestión de proyectos

Inglés avanzado (C1 - C2)

Trabajo en equipo

Educación

Título en disciplina científica o de salud

Herramientas

Pleasereview

Descripción del empleo

The Manager, Program Excellence supports the Director, Evidence Generation Program Excellence in managing and prioritizing USMA departmental applications/functions. Responsible for department-level activities with a tactical approach, requiring multitasking across activities with a focus on clinical trial operations.

About the Role

This role is based in Mexico City. Novartis cannot offer relocation support; please only apply if this location is accessible for you.

Key Responsibilities:

• Manage and execute medical review of concepts, project plans, and protocols for US-MA organization.
• Support development, update, and presentation of training materials related to clinical trial processes.
• Assist in revising and implementing trial submission processes, including QC of submissions, workflow tracking, and milestone monitoring.
• Collaborate with clinical teams and IT to identify, prioritize, and resolve issues, providing timely responses and reports.
• Implement innovative solutions to accelerate data generation activities and assist teams with prioritization questions.
• Work with the Director to define and clarify business processes and requirements for prioritization and metrics tracking.
• Support the development of project plans for annual prioritization activities, including open research questions (ORQs).
• Require advanced English skills (C1 – C2).
• Candidate must have at least 5 years of project management, technical, and operational experience, with 3 years in clinical trial execution, including country and/or global experience.
• Bachelor’s degree in a scientific or healthcare discipline is preferred, especially sciences.
• Experience in managing critical business meetings with cross-functional stakeholders.
• Experience with Pleasereview is recommended.
• Proven ability to work independently and in teams, supporting multiple projects.

Commitment to Inclusion

Novartis is committed to fostering an inclusive, diverse work environment that reflects the communities we serve. We provide reasonable accommodations for individuals with disabilities. To request accommodations, contact [e-mail], including your contact details and the job requisition number.

Why Novartis: Helping people with disease requires innovative science and a community of passionate people. Join us to make a difference: https://www.novartis.com/about/strategy/people-and-culture

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