Descrição da Vaga
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 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)
Master's 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.
Medical
Ready to Apply?
Don't miss this opportunity! Apply now and join our team.
Detalhes da Vaga
Data de Publicação:
March 1, 2026
Tipo de Vaga:
Artes e Entretenimento
Localização:
Brazil
Company:
Pfizer
Ready to Apply?
Don't miss this opportunity! Apply now and join our team.