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Pharmacovigilance Associate Ii

2-3 years
Not Disclosed
10 Jan. 31, 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
📍 Location: Bangalore, India
🕒 Experience: 2-3 years in pharmacovigilance
💼 Company: Teva Pharmaceuticals

About Teva

Teva Pharmaceuticals is on a mission to make good health more affordable and accessible. As the world’s leading manufacturer of generic medicines, Teva is committed to improving lives worldwide. With over 200 million people using their medicines every day, Teva is constantly striving to make a meaningful impact.

Role Overview

The Pharmacovigilance Associate II will support the aggregate reports preparation process, generating and collecting data, and authoring relevant sections of reports. This role also includes QC support, case data verification, and collaboration with peers, writers, and stakeholders.

Key Responsibilities

Report Generation: Generate required reports (line listings, summary tabulations) from PV database and BI platforms.
Data Collection & Authoring: Collect and assimilate data to support the preparation of aggregate reports, along with authoring relevant sections of the reports.
Case Data Verification: Ensure case completeness in the PV database by raising correction requests to relevant teams.
QC of Reports: Review and perform quality control (QC) of data collection, report generation, and authoring for assigned reports.
Lead Projects: Act as a topic lead for selected parts of the process and projects.
Mentoring & Coaching: Coach and mentor junior team members.
Stakeholder Communication: Draft responses to queries from stakeholders and regulatory agencies.
Documentation: Maintain and author training documents and working procedures.
Collaboration: Foster collaborative relationships with peers, writers, and functions within the organization.

Qualifications

🎓 Education:

  • University degree in BDS, BAMS, BHMS, Pharm.D, M.Pharm (Pharmacy Practice, Pharmacology, Regulatory Affairs), or equivalent.
    💼 Experience:
  • 2-3 years of experience in pharmacovigilance, including medical writing and/or ICSR/case processing.
  • Experience in periodic reports preparation is a plus.

Mode of Work

This position is on-premise.

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