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IQVIA Hiring Pharmacovigilance Operations Coordinator 1

Published on

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

Kochi & Kolkata

1 years

Verified Job

Online Application

IQVIA is a globally recognized leader in clinical research, pharmacovigilance, and healthcare intelligence, supporting life sciences companies in developing and commercializing innovative medical treatments worldwide. With a strong presence in India, IQVIA offers robust career growth in Lifecycle Safety, Drug Safety Operations, and Clinical Research Services.


πŸ“Œ Job Overview – Operations Coordinator 1

IQVIA is inviting applications for the position of Operations Coordinator 1 to support Lifecycle Safety service lines, including Safety Operations (SO) and Lifecycle Safety Management (LSM). This role is ideal for candidates seeking entry-level to early-career opportunities in pharmacovigilance operations and safety data management.

Job Location:

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  • Kochi, Kerala
  • Kolkata, West Bengal

Employment Type: Full-time
Last Date to Apply: January 8, 2026


🧩 Key Responsibilities

As an Operations Coordinator at IQVIA, you will:

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  • Assist in processing Adverse Events (AE) and endpoint data, including intake, tracking, and workflow distribution
  • Track safety case timelines and ensure timely submissions to clients and stakeholders
  • Support Lifecycle Safety database entry, quality control, and report generation
  • Coordinate safety report submissions to regulatory authorities and investigators
  • Maintain project files, case folders, and document control systems
  • Assist with project start-up activities, system access, and administrative workflows
  • Archive safety data and manage records post-study closure
  • Support database validation, user testing, and ad-hoc data searches
  • Coordinate meetings, courier dispatch, and administrative logistics
  • Mentor junior administrative staff and support continuous process improvement

πŸŽ“ Qualifications & Skills Required

Education & Experience

  • Degree in Life Sciences, Pharmacy, Healthcare, or allied scientific discipline
  • Minimum 1 year of relevant experience in pharmacovigilance, clinical research, or safety operations

Technical & Professional Skills

  • Good understanding of GCP, ICH guidelines, SOPs, and safety workflows
  • Working knowledge of medical terminology
  • Proficiency in Microsoft Office and web-based applications
  • Strong organizational, multitasking, and time-management skills
  • Excellent written and verbal communication
  • High attention to detail, accuracy, and compliance

πŸ’Ό Why Join IQVIA? (Benefits)

  • Opportunity to build a career in Drug Safety & Pharmacovigilance
  • Exposure to global clinical safety projects
  • Structured training and mentoring programs
  • Collaborative, inclusive, and professional work environment
  • Competitive salary and long-term career growth

Estimated Salary Range: β‚Ή3,00,000 – β‚Ή5,00,000 per annum (industry-aligned, indicative)


πŸ“ How to Apply

Application Link

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