Pfizer is the world’s premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support.
Post : Sr. Associate – Safety Surveillance
Position Purpose
Review, preparation, and completion of reports of adverse drug experiences, to determine the safety profile of Pfizer’s products and to meet regulatory requirements.
Job Description
Identify and select routine cases for processing, determining appropriate prioritization criteria, and noting reasons for any delays.
Assess cases to distinguish those with particular complexities and/or specific issues and escalate appropriately.
Review, rank, verify, process and document: event terms; case classifications (validity, seriousness, expectedness / listedness / labeledness); special scenarios; product complaint information; reportability with due date; and accuracy and consistency. Based on assessment of cases, process accordingly.
Review case criteria 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.
Candidate Profile
Experience and skill with medical writing an advantage.
Minimum a Bachelor’s degree in pharmacy, dental science, or equivalent; healthcare professional qualification is mandatory.
0-6 years of experience in Pharmacovigilance.
Additional Information
Experience : 0-6 years
Qualification : Bachelor’s degree in pharmacy
Location : Chennai
Industry Type : Pharma / Healthcare / Clinical research
End Date : 30th September 2024
