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Pv Professional

2-4 years
Prefered by Company
10 Nov. 20, 2024
Job Description
Job Type: Full Time Education: M.Pharm/ Pharm.D/ BDS Postgraduate in registered life Sciences 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

Who We Are
At Teva Pharmaceuticals, we are on a mission to make good health more affordable and accessible, helping millions around the world enjoy healthier lives. This shared purpose connects our diverse team across nearly 60 countries, representing a rich variety of nationalities and backgrounds.

As the world’s leading manufacturer of generic medicines and the proud producer of numerous products on the World Health Organization’s Essential Medicines List, we impact over 200 million lives daily. While this number is remarkable, we continuously seek innovative ways to make a difference and welcome passionate individuals to join us in this journey.


Your Role: How You’ll Spend Your Day
You will play a pivotal role in ensuring patient safety through your contributions in pharmacovigilance case processing and operations. Key responsibilities include:

  • Adverse Event Processing:

    • Manage serious and non-serious adverse events from post-marketing sources.
    • Ensure accurate and consistent medical coding using MedDRA (Medical Dictionary for Regulatory Activities) for all events in the Safety Database.
    • Perform data verification between source documents and entered data to evaluate events, suspect drug coding, seriousness, causality, listedness, and narrative writing.
    • Assess the need for follow-ups and queries to ensure accurate data transfer.
  • Process Quality & Compliance:

    • Analyze quality data for trend identification to support process stabilization.
    • Meet compliance metrics, including case timelines, assigned training completions, and turnaround times (TAT) for activities.
    • Ensure process transparency through effective communication with internal (departments and units) and external (partners, authorities, vendors) stakeholders.
  • Support Activities:

    • Provide administrative support for Safety Database-related activities in alignment with work instructions and GVP modules.
    • Assist in audits and inspections by investigating and analyzing trends.
    • Mentor and train new hires, ensuring knowledge transfer and progress monitoring during their learning phase.

Your Experience and Qualifications

  • Education:
    • M.Pharm, Pharm.D, or BDS Postgraduate in Life Sciences.
  • Experience:
    • 2–4 years of relevant experience in pharmacovigilance case processing and patient safety operations.

Our Commitment to Equal Opportunity
Teva Pharmaceuticals is dedicated to fostering an inclusive workplace and providing equal employment opportunities for all. We prohibit discrimination based on 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 recognized status.

We are committed to accommodating individuals throughout the recruitment process. If contacted for a job opportunity, please inform us of any required accommodations. All provided information will remain confidential and be used solely to ensure an accessible candidate experience.

Join us in making a difference—every day, for millions around the globe.