Are you looking for a career in Pharmacovigilance (PV)? IQVIA, a global leader in clinical research and healthcare intelligence, is hiring for multiple Pharmacovigilance roles in Pune. If you have a background in life sciences and experience in drug safety, this is an excellent opportunity to grow your career with a top-tier organization.
Available Pharmacovigilance Job Roles at IQVIA Pune
1. Safety Associate
Experience: 1-1.5 years
Qualifications: Bachelor’s degree in life sciences or related field
Key Responsibilities:
- Review and process safety data from various sources.
- Perform pharmacovigilance activities including adverse event (AE) tracking, database entry, coding, and narrative writing.
- Ensure compliance with regulatory guidelines and SOPs.
- Assist in training new team members.
Skills Required:
- Basic knowledge of medical terminology and pharmacovigilance databases.
- Strong attention to detail and communication skills.
2. Operations Specialist 1
Experience: Up to 3 years (including 1 year in PV)
Qualifications: Bachelor’s degree in life sciences or related field
Key Responsibilities:
- Process safety data and perform AE case processing.
- Ensure compliance with project timelines and quality standards.
- Liaise with project teams and healthcare professionals.
- Support medical review of non-serious AEs/ADRs.
Skills Required:
- Intermediate knowledge of safety databases and regulatory requirements.
- Strong organizational and time management skills.
3. Operations Specialist 2
Experience: Up to 5 years (including 3 years in PV)
Qualifications: Bachelor’s degree in life sciences or related field
Key Responsibilities:
- Lead safety data processing and pharmacovigilance activities.
- Oversee regulatory reporting (expedited and periodic).
- Mentor junior team members and support process improvements.
- Conduct medical reviews for AEs/ADRs.
Skills Required:
- Advanced knowledge of pharmacovigilance regulations.
- Strong leadership and problem-solving skills.
4. Associate Manager, Safety Operations
Experience: Up to 6 years (including 4 years in PV & 2 years in management)
Qualifications: Bachelor’s degree in life sciences or related field
Key Responsibilities:
- Supervise PV teams and ensure compliance with SOPs.
- Manage resource allocation, training, and performance reviews.
- Support global pharmacovigilance initiatives.
- Drive process improvements and quality standards.
Skills Required:
- Strong leadership and team management skills.
- Expertise in pharmacovigilance regulations and safety databases.
About IQVIA
IQVIA is a world leader in clinical research, healthcare data analytics, and pharmacovigilance services. With a presence in over 100 countries, IQVIA helps biopharmaceutical companies accelerate drug development and improve patient outcomes through intelligent data-driven solutions.
Application Link
📌 Apply for Safety Associate Role
📌 Apply for Operations Specialist 1 Role
📌 Apply for Operations Specialist 2 Role
📌 Apply for Associate Manager Role
