Use Your Power for Purpose

At Pfizer, our Worldwide Safety colleagues are pivotal in bridging evidence-based medical decision support with stakeholders to enhance health and treatment outcomes. Whether you are developing frameworks to ensure our evidence is scientifically robust, offering unbiased and medically essential expertise, or exploring ways to address data gaps, our mission remains clear: to empower healthcare decisions regarding the safe and appropriate use of medicines for patients.

What You Will Achieve

In this role, you will:

Monitor the company's drug, biologics, and medical devices surveillance program.

Intake, evaluate, and process adverse reports for both clinical trials and post-marketing activities.

Make decisions within limited options to resolve problems, under the supervisor's direction.

Work in a structured environment, following established procedures.

Ensure work is regularly reviewed for technical judgment, completeness, and accuracy.

Provide expertise on regulatory requirements and corporate policies for regulatory submissions to project teams.

Support Worldwide Strategy and Regulatory teams by analyzing post-marketing safety data, reviewing medical literature, and related activities.

Determine the appropriate workflow for case processing by reviewing case criteria.

Qualifications

Must-Have

Bachelor's Degree in Pharmacy or Medical

Strong skills in productivity, organizational and time management in order to meet strict regulatory compliance goals

Fluent in spoken and written English

Nice-to-Have

Master's Degree in Pharmacy or Medical

Relevant pharmaceutical industry experience

Work Location Assignment: Hybrid

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.