Pfizer Hiring Safety Data Management Specialist

Pfizer Hiring Safety Data Management Specialist

5 June, 2022

Job Description

  • Contribute to completion of project milestones and organize own work to meet project task deadlines.
  • Provide project teams with expertise on regulatory requirements and corporate policies governing documents for regulatory submission.
  • Support Worldwide Strategy and Regulatory teams by providing analyses of post-marketing safety data, reviews of the medical literature, and similar related activities.
  • Review case criteria to determine the appropriate workflow for case processing.

Qualifications

Qualifications

Must-Have

ONLY B. Pharm qualification.

Direct work experience in Pharmacovigilance, ICSR (Individual Case Safety Reports) processing of NO MORE THAN 2 years. B. Pharm freshers are also welcome to apply.

Decent knowledge of pharmacovigilance regulations, solid analytical skills, and very keen attention to detail!

Nice-to-Have

Direct experience in the ARGUS safety database and with E2B case processing.

Good academic and/or extra-curricular accomplishments.

Apply through this Link

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