Instagram
youtube
Facebook

Pharmacovigilance Associate Ii

2-3 years
3-4 lakh per annum
10 Jan. 31, 2025
Job Description
Job Type: Full Time Education: DS/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

πŸ“Œ Pharmacovigilance Associate II | Teva Pharmaceuticals
πŸ“ Location: Bengaluru, India
πŸ—“ Posted: January 21, 2025
πŸ’Ό Job ID: 60345

🌍 About Teva Pharmaceuticals

Teva Pharmaceuticals is committed to making good health more affordable and accessible to people across the globe. With operations in nearly 60 countries, we produce generic medicines and essential products listed by the World Health Organization, reaching over 200 million people every day. Our mission is to help millions of individuals enjoy healthier lives, and we are constantly looking for new talent to make that mission a reality.

πŸ“ About the Role

As a Pharmacovigilance Associate II, your role is integral to supporting the aggregate reports preparation process. You will generate and collect the required data for report preparation, author relevant sections of the reports, and ensure quality control throughout the process.

πŸ” Key Responsibilities

Report Generation & Data Collection

βœ” Generate required reports (line listings, summary tabulations) from PV database and BI platforms for assigned reports.
βœ” Collect and assimilate data to support writers in report preparation, including authoring relevant sections.
βœ” Ensure case completeness within the PV database, raising correction requests as necessary.

Quality Control & Collaboration

βœ” Perform QC for the data generation, collection, and authoring of assigned reports.
βœ” Act as a topic lead for selected parts of the process or specific projects.
βœ” Mentor and develop junior staff within the team.
βœ” Collaborate with peers, writers, and other functions within Teva.

Training & Reporting

βœ” Draft responses to queries from stakeholders and regulatory agencies as required.
βœ” Maintain training documents and working procedures for the team.
βœ” Ensure periodic reports are performed in line with relevant procedures.

πŸ“‹ Qualifications

πŸŽ“ Education: University degree in BDS, BAMS, BHMS, Pharm.D, M.Pharm (Pharmacy Practice/Pharmacology/Regulatory Affairs).
πŸ“Œ Experience: 2-3 years of experience in Pharmacovigilance, including medical writing and/or ICSR/case processing. Previous experience with periodic reports is preferred.
πŸ“Œ Skills: Strong collaboration skills, attention to detail, and the ability to work with cross-functional teams.

🌟 Equal Opportunity Commitment

Teva Pharmaceuticals is committed to a diverse and inclusive workplace, providing equal employment opportunities without regard to age, race, religion, gender, disability, or other legally recognized statuses.

πŸ“© Apply Now