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IQVIA Hiring for Pharmacovigilance (JLPT)

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IQVIA

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences

Thane, Maharashtra

0 - 3 Years

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IQVIA, a global leader in clinical research and healthcare intelligence, is hiring an Operations Specialist 1 JLPT in Thane, Maharashtra. This role is ideal for healthcare or life sciences graduates looking to kickstart a career in pharmacovigilance, safety data management, and clinical research operations. Join a dynamic team where you will contribute to improving patient safety and regulatory compliance.


Key Responsibilities

As an Operations Specialist 1, you will:

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  • Review, assess, and process safety data from multiple sources, ensuring compliance with regulations, SOPs, and internal guidelines.
  • Collect and track Adverse Events (AE) and endpoint information.
  • Perform database entry, AE/product coding, narrative writing, and literature review as per project timelines.
  • Ensure productivity, quality, and delivery standards across project requirements.
  • Liaise with functional teams, healthcare professionals, and clients to address project-related issues.
  • Mentor new team members and support departmental initiatives.
  • Conduct medical review of non-serious AEs and ADRs, including coding, causality assessment, and documentation.
  • Participate in team meetings, provide feedback, and ensure adherence to training plans and SOPs.

Required Qualifications

  • Bachelor’s degree in Scientific, Healthcare, or Life Sciences discipline.
  • Up to 3 years of relevant experience or equivalent combination of training and education.
  • Strong knowledge of medical terminology, pharmacovigilance, and safety databases.
  • Working knowledge of global and local clinical research regulations.
  • Proficiency in Microsoft Office and web-based applications.
  • Strong organizational, communication, and problem-solving skills.
  • Ability to multitask, meet deadlines, and work independently or in teams.
  • Flexibility to work shifts and occasional travel as required.

Benefits

  • Opportunity to work with a global leader in clinical research and healthcare intelligence.
  • Hands-on experience in pharmacovigilance and safety data operations.
  • Professional growth and skill development across clinical and regulatory functions.
  • Collaborative and inclusive work environment.

How to Apply

Application Link

IQVIA Hiring for Pharmacovigilance (JLPT)
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