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Pharmacovigilance Associate I

1-2 years
Not Disclosed
10 July 29, 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

About Us

At Teva Pharmaceuticals, our mission is to make healthcare more affordable and accessible, improving the lives of millions globally. With a presence in nearly 60 countries, we unite people from diverse backgrounds and cultures. As the leading manufacturer of generic medicines and a key contributor to the World Health Organization’s Essential Medicines List, we impact the lives of over 200 million people daily. We’re always searching for new ways to make a difference and welcome passionate individuals to join us in this mission.

Role Overview

As a key member of our team, you will:

  • Data Retrieval: Gather and prepare data for authoring specific sections of Periodic Safety Update Reports (PSURs).
  • Quality Control: Review and ensure the accuracy of data retrieval processes and selected PSUR sections.
  • PSUR Finalization: Finalize PSURs, including creating the final PSUR PDFs.
  • Regulatory Responses: Draft responses to requests from regulatory agencies as needed.
  • Compliance: Ensure that all PSUR-related activities are performed according to established procedures.
  • Collaboration: Work closely with other functions within Teva to support your role.

Qualifications

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

Reports To

  • Position: PV Manager, Aggregate Reports Expert

Already a Teva Employee?

If you are a current Teva employee, please apply through the internal career site on "Employee Central" for priority consideration. You can also view exclusive opportunities available only to Teva employees. Access the internal career site here: [Internal Career Site]

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Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to providing equal employment opportunities 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 dedicated to fostering a diverse and inclusive workplace. If you need any accommodations during the recruitment process, please let us know so we can support you. All accommodation information will be kept confidential and used solely to provide an accessible candidate experience.