Vaccine Medical Manager

Pfizer; Ciudad de México; Híbrido; MXN 200,000 - 400,000; Jornada completa

Descripción de la vacante

A global pharmaceutical company seeks a dedicated medical professional for a key role in Mexico City. The ideal candidate will have medical expertise in the vaccine portfolio, strong project management capabilities, and proficiency in Microsoft Office. Responsibilities include developing medical strategies, providing technical information, and leading cross-functional projects. A minimum of 6 years of experience in a relevant role is required. This position offers a chance to impact healthcare positively while working in a collaborative environment.

Formación

• Comprehensive understanding of the health environment.
• Deep knowledge of local Codes of Practice, regulations, and guidelines.
• Knowledge of pharmacovigilance and regulatory legislation.

Responsabilidades

• Develop and lead complex projects ensuring productivity and client satisfaction.
• Provide medical and technical information about drug products.
• Develop medical strategies supporting product lifecycle management.

Conocimientos

Medical experience specifically within the vaccine's portfolio

Ability to work independently and manage multiple projects

Proficiency with Microsoft Office

Excellent verbal and written communication skills

Educación

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

Descripción del empleo

Use Your Power for Purpose

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. Whether you are developing the framework to ensure our evidence is scientifically robust, providing unbiased and medically necessary expertise, or exploring ways to close data gaps, our mission remains clear. 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, we strive to enhance healthcare outcomes.

What You Will Achieve

In this role, you will:

• 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.

Here Is What You Need (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
• Medical experience specifically within the vaccine's 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

Bonus Points If You Have (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 end date: DEC 16th, 2025

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 (Equal Employment Opportunity) & Employment Eligibility

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.