Safety Surveillance Associate

eria to determine the appropriate workflow for case processing.

• Write and edit the case narrative.

• Generate reports, ensuring adherence to regulatory compliance timelines.

• Determine appropriate case follow-up, requesting follow-up letters when appropriate.

• Liaise with key partners, including Pfizer Country Organizations, Clinical Development, License Partners, and other stakeholders regarding safety data collection and data reconciliation.

• Develop and maintain expertise and knowledge of all products within the Pfizer portfolio; applicable corporate and global regulations, guidelines, Standard Operating Procedures and writing practices; data entry conventions; and search functions in the safety database.

• Consistently apply regulatory requirements and Pfizer policies.

• 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.

• Ability to achieve personal objectives while meeting departmental standards of performance.

• Ability to work under supervision in a matrix organization.

• Excellent oral and written communication skills.

• Fluency in spoken and written English; knowledge of additional language(s) an advantage.

• Experience and skill with medical writing an advantage.

• Qualifications (i.e., preferred education, experience, attributes):

• 0-4 year's experience in Pharmacovigilance/ Clinical research/ Hospital practice / Teaching etc.

• Mandatory of minimum bachelor's in health care degree (ie, dentistry, pharmacy, nursing, or equivalent).

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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