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Pharmacovigilance Associate I

1-2 years
Not Disclosed
10 July 26, 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, our mission is to make good health more affordable and accessible, helping millions around the globe lead healthier lives. This mission unites our diverse team, spanning nearly 60 countries and encompassing a wide range of nationalities and backgrounds. We are proud to be the world's leading manufacturer of generic medicines and the producer of many products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people worldwide rely on our medicines daily. While this is a remarkable achievement, we are always striving to find new ways to make a difference and welcome new people to join us in this endeavor.

How You’ll Spend Your Day

  • Data Retrieval: Author and prepare selected sections of Periodic Safety Update Reports (PSURs).
  • Review and Quality Control: Oversee the data retrieval process and review selected PSUR sections for quality and accuracy.
  • PSUR Finalization: Create and finalize PSURs, including generating PDF versions.
  • Regulatory Responses: Draft responses to inquiries from regulatory agencies as needed.
  • Compliance: Ensure all PSUR-related activities are conducted in accordance with established procedures and timelines.
  • Collaboration: Work collaboratively with other functions within Teva.
  • Additional Tasks: Perform other duties as assigned by your direct manager.

Your Experience and Qualifications

  • Education: University degree (B.Pharm, M.Pharm, Pharm.D)
  • Language Skills: Proficient in English, both written and spoken
  • Database Experience: Experience with databases such as ARISg, Argus, Cognos, Veeva, TrackWise, QlikSense
  • MS Office Skills: Proficiency in Word, Excel, PowerPoint
  • Experience: Minimum 1-2 years of experience in Pharmacovigilance (PSUR/RMP/PADER writing or ICSR/case processing writing)
  • Skills: Strong sense of compliance and ability to meet deadlines

Reports To

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

Already Working at Teva?

If you are currently employed by Teva, please apply through the internal career site available on "Employee Central." Doing so will prioritize your application and allow you to see opportunities exclusive to Teva employees. Use the following link to search and apply: Internal Career Site. If you experience any issues accessing your Employee Central account, please contact your local HR or IT partner.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is dedicated to providing equal employment opportunities. Our global policy ensures equal opportunity regardless of 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 committed to creating a diverse and inclusive workplace. If you are 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 only to ensure an accessible candidate experience.