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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 good health more affordable and accessible, enhancing the quality of life for millions around the globe. Our commitment unites us across nearly 60 countries, blending diverse nationalities and backgrounds. As the world’s leading manufacturer of generic medicines and a key producer of many products on the World Health Organization’s Essential Medicines List, we touch the lives of at least 200 million people daily. We are always seeking innovative ways to make a difference and invite new talent to join us in this impactful journey.

Your Role

In this position, you will:

  • Data Retrieval: Retrieve and prepare data for authoring selected Periodic Safety Update Reports (PSURs).

  • Review and Quality Control: Review and perform quality control on the data retrieval procedures and selected PSUR sections.

  • PSUR Finalization: Finalize PSURs, including the creation of PSUR PDFs.

  • Regulatory Responses: Draft responses to requests from regulatory agencies as needed.

  • Compliance: Ensure all PSUR-related activities are conducted in accordance with established procedures.

  • Collaboration: Foster collaborative relationships with other functions within Teva.

  • Additional Tasks: Perform other tasks as assigned by your direct manager.

Qualifications

  • Educational Background: 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 sense of compliance and ability to meet deadlines.

Reports To

  • Position: PV Manager, Aggregate Reports Expert

Already Working at Teva?

If you are a current Teva employee, please apply through our internal career site on "Employee Central" to have your application prioritized. You can also access opportunities exclusively available to current Teva employees. Use the following link to search and apply: [Internal Career Site]

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Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to providing equal employment opportunities 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 require any accommodations during the recruitment process, please let us know so we can provide the necessary support. All accommodation information will be handled confidentially and used solely to facilitate an accessible candidate experience.