Pfizer Safety Surveillance Associate Recruitment – Apply Online
Pfizer safety job opening 2021. Pharma job opening 2021. Pfizer announces job opening for pharma candidates. B Pharma job opening 2021. Pharmacy job opening 2021. Pharma job opening 2021. Candidates with a bachelor’s in pharmacy may apply for the job opening at Pfizer. Check out all the details on the same below:
Job Title: Safety Surveillance Associate
Location: India – Chennai
Eligibility Criteria:
- Bachelor’s degree in a science-related field, pharmacy 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.
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 the additional language(s) an advantage.
- Experience and skill with medical writing an advantage.
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.Primary Responsibilities
- 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.
- 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 an 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.
- Â Liaise with key partners, including Pfizer Country Organizations, Clinical Development,
- License Partners, and other stakeholders regarding safety data collection and data reconciliation.
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