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Safety Data Management Specialist

Review, preparation, and completion of reports of adverse drug experiences, to determine the safety profile of Pfizer’s products and to meet regulatory requirements. Determination of local submission of individual and, where appropriate, aggregate safety reports

  • Carry 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 policies
  • Participate, as appropriate, in local, internal and external safety activitie

Technical Skill Requirements:

  • Experience in pharmacovigilance and/or data management preferred but not required
  • Experience and skill with medical writing an advantage
  • Demonstrated computer literacy
  • Experience in use and management of relational databases preferred

Qualifications

  • Health Care Professional or equivalent experience 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 in a matrix organization
  • Fluency in spoken and written English

Closing date for this role is 28th February 2018

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Uanset, hvilken vej du har valgt, har Pfizer en karriere til dig

Hos Pfizer går vi op i at skabe et miljø, hvor vores kolleger kan få succes, samtidig med at vi bidrager til at forbedre verdenssundheden. Vi kommer som videnskabsfolk, chefer, som producenter. Vi er topledere og nyuddannede. Men uanset, hvor vi kommer fra og hvor vores karriere fører os hen, så har vi et fælles mål. At gøre verden til et sundere sted.

Aktuelt søger vi nye medarbejdere inden for alle områder af vores virksomhed og over hele verden. Pfizer er en global virksomhed med ressourcer, der er dedikeret til at udvikle mange forskellige former for medicin til mange forskellige helbredsproblemer, og vi tilbyder karrieremuligheder inden for alle forretningens sundhedsområder samt vores interne og eksterne divisioner.

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