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Pharmacovigilance Associate I

1-2 years
Not Disclosed
10 July 25, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, 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

Who We Are

At Teva Pharmaceuticals, we are dedicated to making good health more affordable and accessible, helping millions worldwide lead healthier lives. Our mission unites a diverse team spanning nearly 60 countries, representing a wide array of nationalities and backgrounds. Working with us means joining the world’s leading manufacturer of generic medicines and the proud producer of numerous products on the World Health Organization’s Essential Medicines List. Every day, at least 200 million people around the world rely on our medicines. While this is an impressive number, we are always seeking new ways to make a difference and welcome new people who share our vision.

How You’ll Spend Your Day

  • Retrieving data for authoring and preparing selected sections of Periodic Safety Update Reports (PSURs).
  • Reviewing and quality checking the data retrieval process and selected PSUR sections.
  • Finalizing PSURs, including the creation of PDF documents.
  • Drafting responses to inquiries from regulatory agencies as needed.
  • Ensuring that assigned PSUR-related tasks are performed in accordance with established procedures.
  • Collaborating with other functions within Teva to ensure seamless operations.

Your Experience and Qualifications

  • A university degree in Pharmacy (B.Pharm, M.Pharm, Pharm.D) or a related field.
  • Proficient in English, both written and spoken.
  • Experience working with databases such as ARISg, Argus, Cognos, Veeva, TrackWise, QlikSense.
  • Proficiency in MS Office, including Word, Excel, and PowerPoint.
  • A minimum of 1-2 years of experience in Pharmacovigilance, particularly in PSUR/RMP/PADER writing or ICSR/case processing.
  • A strong commitment to compliance and meeting deadlines.

Reports To

This position reports to the Pharmacovigilance Manager, Aggregate Reports Expert.

Already Working @TEVA?

If you are currently employed at Teva, please apply through the internal career site available on "Employee Central". This ensures your application is prioritized and allows you access to opportunities exclusive to Teva employees. You can access the internal career site from your home network. If you encounter any issues with your EC account, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to providing equal employment opportunities. Our global policy ensures that employment decisions are made without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin, or any other legally protected status. We are dedicated to fostering a diverse and inclusive workplace for all. If contacted for a job opportunity, please inform us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information will be kept confidential and used solely to provide an accessible candidate experience.