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The Role
Position Purpose
Review, preparation, and completion of clinical study and compassionate sourced adverse event (AE)/serious adverse event (SAE) reports, to determine the safety profile of Pfizer's products and to meet regulatory requirements .
Primary Responsibilities
Technical Skill Requirements
Qualifications (i.e., preferred education, experience, attributes)
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
#LI-PFE
Review, preparation, and completion of clinical study and compassionate sourced adverse event (AE)/serious adverse event (SAE) reports, to determine the safety profile of Pfizer's products and to meet regulatory requirements .
Primary Responsibilities
- Carry out case book-in, data entry and processing activities.
- Assess cases to distinguish those with particular complexities and/or specific issues, and escalate appropriately.
- Identify and select cases for data entry, determining appropriate prioritization criteria, and noting reasons for any delays
- Review, rank, process and document case-related information: event terms; case classifications (validity, seriousness, expectedness/ listedness / labeledness ), special scenarios, product complaint information, reportability with due date; and accuracy and consistency . Based on case assessment, forward the case to the appropriate workflow .
- Write and edit the case narrative.
- Review processed cases to verify accuracy, consistency, and compliance with process requirements, and review case data for special scenarios.
- Consistently apply regulatory requirements and Pfizer policies to determine reportability of scheduled reports, generate reports, and ensure adherence to regulatory compliance timelines.
- Determine and perform appropriate case follow-up, including generation of follow-up request letters when appropriate .
- Liaise with key partners, including Global Pharmacovigilance Organization, Pfizer Safety Surveillance and Reporting Centers of Excellence, Clinical Development, License Partners, and other stakeholders regarding clinical study and compassionate use sourced AE/SAE collection, data reconciliation, and AE/SAE distribution/submission . Participate, as appropriate , in internal and external safety activities.
- Develop and maintain expertise and knowledge of all products within the Pfizer portfolio, applicable corporate and global regulations, guidelines, Standard Operating Procedures and written practices, data entry conventions, and search functions in the safety database.
Technical Skill Requirements
- Experience in pharmacovigilance, in clinical care, or in clinical or scientific research is an advantage but not a requirement.
- Demonstrated computer literacy, particularly in the use and management of relational databases.
- Excellent oral and written communication skills.
- Fluency in spoken and written English; knowledge of additional language(s) an advantage.
Qualifications (i.e., preferred education, experience, attributes)
- Bachelor's degree in a science-related field, pharmacy, nursing, or equivalent; healthcare professional qualification preferred
- 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 ina matrix organization.
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
#LI-PFE
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The Company
What We Do
Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.
Why Work With Us
We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.
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Pfizer Offices
Hybrid Workspace
Employees engage in a combination of remote and on-site work.
Typical time on-site:
Not Specified
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