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Pv Professional

2 - 4 years
Not Disclosed
10 Nov. 30, 2024
Job Description
Job Type: Full Time Education: M.Pharm/ Pharm.D/ BDS Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, 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

Job Title: Pharmacovigilance Case Processor

Location: Bangalore, India
Company: Teva Pharmaceuticals
Job ID: 58167
Date: Nov 15, 2024


About Teva Pharmaceuticals

At Teva, we’re on a mission to make good health more affordable and accessible to millions globally. As the world’s leading manufacturer of generic medicines, we take pride in producing products featured on the World Health Organization’s Essential Medicines List. Today, over 200 million people rely on our medicines daily, and we're continually looking for new ways to make a positive difference in the world.

We are committed to a diverse and inclusive workplace where every individual’s contributions are valued. With employees across nearly 60 countries, we provide a dynamic environment where you can help shape the future of healthcare.


Key Responsibilities

As a Pharmacovigilance Case Processor, your daily activities will include:

  • Processing Adverse Events: Handling both serious and non-serious adverse events from post-marketing sources.

  • Medical Coding: Using MedDRA (Medical Dictionary for Regulatory Activities) to ensure accurate and consistent coding of events in the Safety Database.

  • Data Verification: Verifying source documents and entered data for accuracy, particularly for event coding, seriousness, causality, and listedness.

  • Follow-ups & Query Management: Evaluating the need for follow-up and coordination with stakeholders to ensure accurate data transfer.

  • Reporting & Communication: Maintaining effective communication with internal and external stakeholders for transparent and efficient operations.

  • Administrative Support: Assisting in case processing and safety database-related tasks, ensuring compliance with GVP (Good Pharmacovigilance Practices).

  • Quality Monitoring: Ensuring case processing quality and identifying trends for process improvement.

  • Compliance & Metrics: Ensuring compliance with timelines, training requirements, and other key performance metrics.

  • Mentorship: Providing training and support to new hires, guiding them through the case processing process to ensure accuracy.


Qualifications & Experience

  • Educational Qualifications:

    • M.Pharm, Pharm.D, BDS, or any postgraduate degree in Life Sciences.

  • Experience:

    • 2-4 years of relevant experience in Pharmacovigilance case processing and related activities.

    • Familiarity with patient safety operations and compliance with industry regulations.


Why Teva?

  • Global Impact: Work with a company that reaches over 200 million people worldwide.

  • Professional Development: Gain hands-on experience in the growing field of Pharmacovigilance and drug safety.

  • Inclusive Culture: Be part of a diverse and inclusive team that values equal opportunity for all employees.


Teva Pharmaceuticals is an Equal Opportunity Employer, and we are committed to diversity in the workplace. If you require accommodations throughout the recruitment process, please inform us, and we will treat your request confidentially.

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