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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, we are dedicated to making good health more affordable and accessible, helping millions worldwide lead healthier lives. Our mission unites our diverse workforce, spread across nearly 60 countries, encompassing a wide range of nationalities and backgrounds. As the world’s leading manufacturer of generic medicines and a producer of many products on the World Health Organization’s Essential Medicines List, we reach at least 200 million people daily with our medicines. While this is a significant achievement, we continuously seek new ways to make a difference and welcome new talent to join us in our mission.

How You’ll Spend Your Day

  • Data Retrieval and Preparation: Author and prepare specific sections of Periodic Safety Update Reports (PSURs).
  • Review and Quality Control: Oversee and review the data retrieval process, ensuring accuracy in selected PSUR sections.
  • PSUR Finalization: Finalize PSURs, including the creation of PDF versions.
  • Regulatory Responses: Draft responses to inquiries from regulatory agencies as required.
  • Compliance: Ensure all assigned PSUR-related activities are carried out in accordance with established procedures and timelines.
  • Collaboration: Foster collaborative working relationships with other functions within Teva.

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: Proficient 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 a current Teva employee, please apply through the internal career site available on "Employee Central." Doing so will prioritize your application and give you access to opportunities exclusive to Teva employees. You can access the internal career site from your home network as well. If you encounter any issues with your Employee Central account, please contact your local HR or IT partner.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to providing equal employment opportunities for all. 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. 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 provided will be treated confidentially and used only to ensure an accessible candidate experience.