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Pharmacovigilance Associate Ii

2-3 years
Not Disclosed
10 Feb. 4, 2025
Job Description
Job Type: Full Time Education: BDS/BAMS/BHMS/Pharm.D/M.Pharm Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Associate II – Bangalore, India (pharmacovigilance-associate-ii-bangalore)

Date: January 21, 2025
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job ID: 60345

About Teva Pharmaceuticals:

Teva Pharmaceuticals is a global leader in generic medicines and a key contributor to the World Health Organization’s Essential Medicines List. With a presence in nearly 60 countries, Teva’s mission is to make healthcare more affordable and accessible to millions of people worldwide.

The Opportunity:

As a Pharmacovigilance Associate II, you will play a crucial role in the aggregate reports preparation process, supporting data generation, collection, and quality control for regulatory submissions. This role also includes mentoring junior team members and collaborating with internal stakeholders.

Key Responsibilities:

  • Generate reports (line listings, summary tabulations) from the PV database and BI platforms for assigned reports.
  • Collect and assimilate data to support writers in report preparation and author relevant sections.
  • Ensure data accuracy by reviewing cases in the PV database and requesting corrections as needed.
  • Assess and separate cases based on formulation, dosage, and indication before report generation.
  • Perform quality control (QC) on data collection, report generation, and authoring.
  • Act as a topic lead for selected projects.
  • Coach, mentor, and develop junior staff.
  • Draft responses to regulatory agencies and stakeholders as needed.
  • Maintain training documents and working procedures related to the team’s responsibilities.
  • Ensure all periodic reports comply with applicable working procedures.
  • Foster collaborative relationships with internal teams and other Teva departments.

Qualifications & Experience:

  • University degree in:
    • BDS, BAMS, BHMS
    • Pharm.D, M.Pharm (Pharmacy Practice, Pharmacology, Regulatory Affairs)
  • 2–3 years of experience in Pharmacovigilance, including:
    • Medical writing
    • ICSR/case processing (including clinical trials)
    • Experience in preparing periodic reports (preferred)

Why Join Teva?

Teva Pharmaceuticals is committed to diversity, inclusion, and equal employment opportunities. The company fosters a workplace that ensures fair treatment regardless of age, race, gender, medical condition, or any legally protected status.

Apply today to be part of a mission-driven team making a global impact on healthcare!