Looking for PV Scientist jobs in India or Pharmacovigilance Scientist jobs in Thane? IQVIA has announced a full-time PV Scientist vacancy at its Thane, Maharashtra office. This is an excellent opportunity for professionals with 2–3 years of pharmacovigilance experience who want to work on aggregate safety reports, signal management, literature surveillance, and regulatory safety documentation for global pharmaceutical clients.

If you’re searching for IQVIA careers, drug safety jobs, pharmacovigilance jobs in Maharashtra, or PV Scientist vacancies in India, this opportunity offers exposure to international regulatory requirements and advanced drug safety operations.

Job Details

About IQVIA

IQVIA is one of the world’s leading providers of clinical research, healthcare analytics, commercial insights, and pharmacovigilance services. The company partners with pharmaceutical, biotechnology, and healthcare organizations worldwide to accelerate drug development while improving patient safety and healthcare outcomes.

Professionals joining IQVIA gain exposure to global regulatory standards, innovative technologies, and international pharmacovigilance programs.

Key Responsibilities

As a PV Scientist, your responsibilities will include:

• Prepare and finalize aggregate safety reports including:
  • PBRER
  • PSUR
  • DSUR
  • PADER
  • Risk Management Plans (RMP)
  • Aggregate Clinical Overviews
• Conduct literature safety surveillance for marketed and investigational products.
• Perform signal detection, validation, evaluation, and risk characterization.
• Author responses to regulatory authority and PRAC safety queries.
• Lead safety management activities for clinical and post-marketing products.
• Collaborate with Regulatory Affairs, Medical Writing, Clinical Research, Quality, Safety Operations, and IT teams.
• Maintain compliance with GVP, GCP, ICH Guidelines, and SOPs.
• Participate in internal and external audits.
• Mentor junior pharmacovigilance professionals.
• Monitor project metrics and ensure timely project delivery.
• Support process improvements and innovation initiatives.

Required Qualifications

Candidates should possess:

• Bachelor’s Degree in a Scientific or Healthcare discipline
• 2–3 years of pharmacovigilance or drug safety experience
• Strong knowledge of:
  • Aggregate Safety Reports
  • Signal Management
  • Benefit-Risk Assessment
  • Medical Terminology
  • Literature Surveillance
• Familiarity with:
  • Good Pharmacovigilance Practice (GVP)
  • Good Clinical Practice (GCP)
  • ICH Guidelines
• Excellent written and verbal communication skills
• Strong analytical and project management abilities
• Proficiency in Microsoft Word, Excel, and PowerPoint
• Ability to work independently and manage multiple priorities

Preferred Skills

Successful candidates will demonstrate:

• Attention to detail
• Scientific writing expertise
• Regulatory documentation experience
• Leadership and mentoring capability
• Time management skills
• Client communication skills
• Decision-making ability
• Cross-functional collaboration
• Problem-solving mindset

Why Join IQVIA?

Working at IQVIA offers several professional advantages:

• Global exposure in pharmacovigilance projects
• Career growth in drug safety and regulatory science
• Opportunities to work with international pharmaceutical clients
• Collaborative work environment
• Continuous professional learning
• Exposure to advanced safety analytics
• Participation in global regulatory compliance initiatives
• Stable career path in life sciences

Salary Expectations

Based on current market trends for PV Scientist jobs in Thane, the estimated annual salary is:

₹8,00,000 – ₹12,00,000 per annum (CTC)

Actual compensation will depend on qualifications, experience, and interview performance.

How to Apply

Application Link