Analista Farmacovigilância Pl

Use Your Power for Purpose

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

In this role you will:

• Monitor and manage the companys 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 Pfizers 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)

• Masters degree

• Relevant pharmaceutical industry experience

• Familiarity with management of performance metrics

• Strong problem-solving skills

• Proficiency in safety database and data mart search functions

• Experience using common AI tools including generative technologies such as ChatGPT or Microsoft Copilot to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices including risk management and ethical use

Other Job Details

• Work Location Assignment:On-site 2-3x/week or as needed by the business

• Last day to apply for job: March 4 2026

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.