IQVIA is a global leader in clinical research, healthcare analytics, and pharmacovigilance services. We support life sciences companies in accelerating drug development, improving patient outcomes, and ensuring regulatory compliance. With a presence in over 100 countries, IQVIA offers career growth, innovation, and impactful work in the healthcare domain.
1. PV Scientist – Kochi & Thane (2 Days Left to Apply!)
Job ID: R1463842
Locations: Kochi, India | Thane, Maharashtra, India
Job Type: Full-time
Last Date to Apply: June 20, 2025
Job Description
IQVIA is seeking a PV Scientist to join our Safety Aggregate Report and Analytics (SARA) Center team. The role involves leading safety aggregate reports, literature surveillance, signal management, and benefit-risk assessments for pharmacovigilance activities.
Key Responsibilities:
- Author and finalize aggregate safety reports (PBRERs/PSURs, DSURs, PADERs, RMPs, ACOs).
- Lead literature surveillance for marketed and investigational products.
- Perform signal detection, validation, and evaluation for risk assessment.
- Respond to regulatory agency/PRAC inquiries and support labeling documents.
- Collaborate with cross-functional teams (Regulatory Affairs, Medical Safety, Clinical Research, etc.).
- Participate in audits, inspections, and process improvements.
- Mentor junior team members and ensure compliance with GVP, ICH guidelines, and SOPs.
Qualifications:
- Bachelor’s degree in Life Sciences, Pharmacy, or Healthcare.
- 2-3 years of pharmacovigilance/safety reporting experience.
- Strong knowledge of GCP, GVP, ICH guidelines.
- Proficiency in Microsoft Office and pharmacovigilance databases.
- Excellent communication, organizational, and project management skills.
2. Manager, Safety Operations – Pune (5 Days Left to Apply!)
Job ID: R1480889
Location: Pune, Maharashtra, India
Job Type: Full-time
Last Date to Apply: June 23, 2025
Job Description
IQVIA is hiring a Manager, Safety Operations to oversee a team handling safety case processing, compliance, and operational metrics in pharmacovigilance.
Key Responsibilities:
- Manage Safety Operations staff, ensuring adherence to timelines and quality standards.
- Conduct bi-monthly meetings to review project status, risks, and training needs.
- Collaborate with Safety Management for resource allocation and workload distribution.
- Support audits, inspections, and bid defenses (RFI/RFP).
- Drive employee engagement, training, and career development initiatives.
- Ensure compliance with SOPs, regulatory guidelines, and corporate training.
Qualifications:
- Bachelor’s degree in Life Sciences or related field.
- 4+ years in Pharmacovigilance + 3 years in Line Management.
- Strong leadership, communication, and problem-solving skills.
- Experience in project finance (EAC, forecasting, risk management).
- Ability to work in shifts (if required) and manage global teams.
How to Apply?
✅ Interested candidates can apply before the deadline:
