Sr.Drug Safety Associate

Pfizer, S.A. de C.V; Ciudad de México; Híbrido; MXN 500,000 - 700,000; Jornada completa

Descripción de la vacante

A global pharmaceutical company located in Mexico City seeks an experienced professional to monitor and manage drug safety surveillance. This role involves evaluating reports, ensuring regulatory compliance, and mentoring team members. A BA/BS or MBA/MS degree is required along with strong organizational and project management skills. Fluency in English is essential. The position offers competitive compensation and must be performed in the office part-time.

Servicios

Competitive compensation

Benefits programs

Formación

• BA/BS with at least 2 years of experience or MBA/MS with any years of experience.
• Strong organizational and project management skills.
• Solid knowledge of global regulations and guidelines for drug development.
• Demonstrated analytical and statistical skills.
• Fluency in spoken and written English.

Responsabilidades

• Monitor and manage the company's drug, biologics, and medical devices surveillance program.
• Intake, evaluate, and process adverse reports for both clinical trials and post-marketing activities.
• Act as a subject matter expert, liaising with partners regarding safety data collection.
• Review and prepare safety-related reports for regulatory compliance.
• Manage safety resources within the local team and mentor colleagues.

Conocimientos

Organizational skills

Project management skills

Analytical skills

Fluency in English

Educación

BA/BS or MBA/MS

Descripción del empleo

Overview

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life-changing medicines to the world.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

Our mission is straightforward: empower healthcare decisions regarding the safe and appropriate use of medicines for patients. Whether you are developing the framework to ensure our evidence is scientifically robust, providing unbiased and medically essential expertise, or exploring ways to bridge data gaps, your role is vital. By ensuring our evidence is sound and offering necessary medical insights, we strive to improve patient care and treatment efficacy.

What You Will Achieve

• Monitor and manage the company\'s drug, biologics, and medical devices surveillance program, ensuring comprehensive oversight.
• Intake, evaluate, and process adverse reports for both clinical trials and post-marketing activities, ensuring accurate and timely handling.
• Act as a subject matter expert, liaising with key partners regarding safety data collection, reconciliation, and ensuring regulatory compliance.
• Review, analyze, prepare, and complete safety-related reports to determine the safety profile of products and meet regulatory requirements.
• Verify the accuracy, consistency, and compliance of processed cases, and review case data for special scenarios, ensuring high standards are maintained.
• Manage safety resources within the local team, provide specific pharmacovigilance or product knowledge, mentor colleagues, and maintain advanced knowledge of Pfizer\'s product portfolio and corporate policies.

Here Is What You Need (Minimum Requirements)

• BA/BS with at least 2 years of experience or MBA/MS with any years of experience
• Strong organizational and project management skills
• Solid knowledge of global regulations and guidelines for drug development
• Demonstrated analytical and statistical skills
• Fluency in spoken and written English

Bonus Points If You Have (Preferred Requirements)

• Relevant pharmaceutical industry experience
• Familiarity with management of performance metrics
• Strong problem-solving skills
• Proficiency in safety database and data mart search functions
• Extensive knowledge of Mexican legislation (NOM-220, NOM-240, and good pharmacovigilance practices)

Other Job Details

• Last Date to Apply for Job: Oct 23rd, 2025.
• Work Location Assignment: Mexito City, Mexico. 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.

Breakthroughs that change patients’ lives

Research confirms what intuition tells us: that purpose-driven companies perform better, are more innovative, attract and retain the best people, and know how to unleash the power of those people. Pfizer’s purpose—Breakthroughs that change patients\' lives—fuels everything we do and reflects our passion for building on our legacy as one of the greatest contributors of good to the world.

Each word in our purpose has meaning and reflects the value we strive to bring to patients and society:

“Breakthroughs” - These are the innovations, scientific and commercial, that we seek to deliver every day. All colleagues, regardless of role, level or location, strive for breakthroughs every day.

“Change” - We want to do more than simply improve patients’ medical conditions; we want to dramatically change their lives for the better.

“Patients’ lives” - We consider not only patients, but everyone they touch—including their families, caregivers, and friends—and everything they love to do. It’s an intentionally holistic view.

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Every decision we make and every action we take is done with the patient in mind—and to nurture an environment where breakthroughs can thrive.

Our Values

To fully realize Pfizer’s purpose, we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

The “how” is represented by four simple, powerful values—courage, excellence, equity, and joy—that define our company and our culture.

Courage: Breakthroughs start by challenging convention, especially in the face of uncertainty or adversity. This happens when we think big, speak up, and are decisive.

Excellence: We can only change patients’ lives when we perform at our best together. This happens when we focus on what matters, agree who does what, and measure our outcomes.

Equity: We believe that every person deserves to be seen, heard, and cared for. This happens when we are inclusive, act with integrity, and reduce healthcare disparities.

Joy: We give ourselves to our work, but it also gives to us. We find joy when we take pride, recognize one another, and have fun.