Vaccine Medical Manager

Pfizer; Xico; Híbrido; MXN 820,000 - 1,185,000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company is seeking a Vaccine Medical Manager in Mexico City, who will manage complex projects and provide technical information about drug products. Candidates should have relevant experience in the vaccine field and strong communication skills. The role involves collaboration with marketing and medical departments to ensure compliance and effective project management, with opportunities for mentoring and training colleagues. This position requires 2-3 days in the office per week.

Formación

• BA/BS with 6+ years of experience or MBA/MS with 5+ years of experience or PhD/JD with 1+ year of experience or MD/DVM with any years of relevant experience.
• Experience specifically within the vaccine portfolio.
• Comprehensive understanding of the health environment.

Responsabilidades

• Develop and lead complex projects, managing plans and ensuring productivity.
• Provide medical and technical information about drug products.
• Review and provide educational materials ensuring they are ethical and compliant.

Conocimientos

Project management

Communication skills

Medical expertise

Independent work

Knowledge of local regulations

Educación

BA/BS with 6+ years of experience or MBA/MS with 5+ years of experience or PhD/JD

Herramientas

Microsoft Office

Descripción del empleo

Vaccine Medical Manager

Location: Mexico City, Mexico
Time type: Full Time
Post expires: December 16th
Work Location Assignment: Mexico City office 2‑3 days per week, or as needed by the business

Overview

Pfizer’s Worldwide Medical and Safety colleagues are essential in bridging evidence‑based medical decision support with colleagues and stakeholders to achieve better health and treatment outcomes. We aim to empower healthcare decisions regarding the safe and appropriate use of medicines for patients by creating a scientifically sound foundation, offering impartial medical expertise, and investigating data deficiencies to enhance healthcare outcomes.

What You Will Achieve

• Develop and lead/co‑lead complex projects, managing plans to achieve objectives and ensuring productivity, quality, and client‑satisfaction goals are met.
• Provide medical and technical information about the company’s drug products to the organization, customers, and the government.
• Review and provide educational, promotional, and formal report‑format materials to various company departments, ensuring all materials are ethical, compliant, and scientifically referenced.
• Develop medical strategies that support product lifecycle management, execute medical plans, and address scientific input for marketed products.
• Provide counsel and expertise to the Marketing Team for program elaboration, strategies, and tactical approaches for the commercial success of drugs.
• Act as the Regional Medical Information contact for local issues, ensuring aligned medical communications with Medical Scientific Relations and addressing potentially problematic medical or clinical issues in promotional materials.
• Collaborate with marketing and medical colleagues to disseminate clinical research data, prepare study reports and manuscripts, and provide analysis of candidate products for licensing and further clinical development.
• Train colleagues on core Medical Information skills, assess their progress, and help them reach their full potential.
• Serve as the subject‑matter expert for Medical Information on responsible products, managing project statuses and budgets, preparing status reports, and developing resolutions to meet objectives.

Minimum Requirements

• BA/BS with 6+ years of experience or MBA/MS with 5+ years of experience or PhD/JD with 1+ year of experience or MD/DVM with any years of relevant experience
• Experience specifically within the vaccine portfolio
• Comprehensive understanding of the health environment
• Deep knowledge of relevant applicable local Codes of Practice, SOPs, regulations, and guidelines
• Knowledge of pharmacovigilance and regulatory legislation and its impact on the product portfolio
• Proficiency with computer and software applications, particularly Microsoft Office
• Ability to work independently and manage multiple projects simultaneously

Preferred Requirements

• Master’s degree (MS/MBA) with 7+ years of experience or a Doctorate Degree (PhD/PharmD/JD)
• Excellent verbal and written communication skills, including scientific writing
• Experience in project management and leading cross‑functional teams
• Ability to interpret internal and external business challenges and recommend best practices for improvements
• Ability to run effective meetings that include diverse opinions and reach consensus
• Experience in training and mentoring colleagues

Posting Information

• Posting end date: December 16th
• Work Location Assignment: Mexico City, must be able to work from assigned Pfizer office 2‑3 days per week, or as needed by the business

EEO Statement

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.