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Clarivate Hiring Pharmacovigilance Specialist
Clarivate Hiring Pharmacovigilance Specialist

Clarivate Hiring Pharmacovigilance Specialist

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Clarivate Hiring Pharmacovigilance Specialist

Meta Description:
Join Clarivate as a Pharmacovigilance Specialist. Ensure safety in pharmaceuticals. Apply now!


Position: Pharmacovigilance Specialist

Organization: Clarivate

Location:

  • Noida, Uttar Pradesh
  • Karnataka

Salary:

  • ₹25,000 – ₹65,000 / month

Qualifications:

  • B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences, Ph.D, MD, Nursing

Experience:

  • 2-3 years

Job Duties and Responsibilities:

  • Conduct structured searches of scientific literature databases (PubMed, Embase, etc.)
  • Screen search results for relevant safety information (adverse events, safety signals, emerging risks)
  • Secondary evaluation of references and index abstracts
  • Provide feedback to primary screeners to improve AE reporting quality
  • Stay updated on new pharmaceutical developments, therapeutic categories, emerging diseases, and biomedical terminology
  • Extract pertinent safety data from selected literature sources
  • Compile and organize extracted data for analysis and review
  • Collaborate with the Pharmacovigilance team to escalate safety signals and ICSRs
  • Evaluate literature reports for potential adverse events or safety concerns
  • Maintain clear documentation of screening activities
  • Prepare summaries of literature findings for internal reporting
  • Ensure accuracy and reliability by adhering to SOPs and quality control measures
  • Communicate findings and safety assessments to internal stakeholders
  • Collaborate with cross-functional teams for timely updates on safety information

Minimum Qualifications:

  • Bachelor’s/Master’s degree in Pharmacy, Life Sciences, Nursing, or related field
  • Advanced degree (e.g., PharmD, MD, PhD) preferred
  • 2-3 years of experience in pharmacovigilance, medical literature analysis, or related field
  • Strong understanding of pharmacovigilance principles, adverse event reporting requirements, and regulatory guidelines
  • Familiarity with scientific literature databases and search techniques (e.g., PubMed, Embase)

Contact:
Apply now on our website or reach out to our recruitment team for more details.

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