Pfizer
DrugSafetyAssociate
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Drug Safety Associate at Pfizer. Skills: drug, biologics, and medical devices surveillance program monitoring, adverse report intake, evaluation, and processing, regulatory requirements expertise, post-marketing safety data analysis, medical literature review. 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.”
Industry & Context.
Make decisions within limited options to resolve problems; analyzing post-marketing safety data; reviewing medical literature
What They're Looking For.
Must Have
Bachelor's Degree in Pharmacy or Medical, 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
What You'll Do.
Monitor the company's drug
and medical devices surveillance program.
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
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.
How You'll Work.
Team & Collaboration
Provide expertise on regulatory requirements and corporate policies for regulatory submissions to project teams.; Support Worldwide Strategy and Regulatory teams
Communication Scope
Fluent in spoken and written English
Full Job Description
**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. Medical
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