Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients.
What You Will AchieveYou will be relied on by the company to monitor its drug, biologics and medical devices surveillance program. This will include intake, evaluation and processing of the adverse reports received. You will support the clinical trial as well as the post marketing activities.
As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.
It is your dedication and hard work that will make it possible for Pfizer’s customers and patients to receive the medicines they need, when they need them.
How You Will Achieve ItCarry out case processing activities.Review, rank, verify, process and document case-related information: event terms; validity, seriousness, special scenarios; timelines; accuracy and consistency. Process cases based on these assessments.Review case criteria to determine appropriate workflow for case processing.Assess cases to distinguish those with particular complexities and/or specific issues and escalate appropriately.Write and edit case narrative.Determine and perform appropriate case follow-up, including generation of follow-up requests.Review processed cases to verify accuracy, consistency and compliance with process requirements, and review case data for special scenarios.Liaise with key partners, locally, and other stakeholders regarding safety data collection and data reconciliation.Develop and maintain expertise and knowledge for applicable corporate and global regulations, for guidelines, Standard Operating Procedures, for data entry conventions, and for search functions in the safety database.Determine reportability of scheduled reports, ensuring adherence to regulatory requirements.Consistently apply regulatory requirements and Pfizer policiesParticipate, as appropriate, in local, internal, and external safety activitiesQualificationsMust-Have
Bachelor's Degree in Health or Life Sciences
Ability, with supervision, to solve routine problems and to surface issues constructively
Ability to make basic decisions with an understanding of the consequences
Ability to achieve personal objectives while meeting departmental standards of performance
Ability to work under supervision in a matrix organization
Demonstrated computer literacy
Fluency in spoken and written English
Nice-to-Have
Health Care Professional or equivalent experience preferred.
1+ years' experience in pharmacovigilance and/or data management preferred but not required
Experience and skill with medical writing an advantage
Experience in use and management of relational databases preferred
Other job details:
Last date to Apply for Job:
Work Location Assignment: This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week.
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
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EEO & 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, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
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Medical