If you are looking to start your career in pharmacovigilance jobs for freshers, this opportunity at IQVIA could be your entry into the clinical research industry. The Operation Coordinator I role in Kolkata focuses on lifecycle safety, adverse event processing, and clinical safety operations—high-demand domains in CROs.
This role is ideal for B.Pharm, M.Pharm, BSc, MSc candidates who want to build expertise in drug safety, AE processing, and regulatory compliance.
Job Overview
- Role: Operation Coordinator I
- Company: IQVIA
- Location: Kolkata, India
- Experience: Freshers (0 years)
- Openings: 15
- Industry: Clinical Research / Pharmacovigilance
Key Responsibilities (Pharmacovigilance & Safety Operations)
- Process and track Adverse Events (AE) and safety data
- Perform lifecycle safety data management activities
- Coordinate safety report submissions to regulatory authorities
- Maintain project documentation and case folders
- Support database entry, QC checks, and report generation
- Assist in safety submission dossiers preparation
- Manage archiving and document control systems
- Track timelines and ensure compliance with safety workflows
- Support project setup, file maintenance, and administrative operations
- Participate in process improvements and workflow optimization
These responsibilities align with core pharmacovigilance roles like ICSR processing and safety reporting.
Eligibility Criteria
Educational Qualification
- B.Pharm / M.Pharm / Pharm.D
- B.Sc / M.Sc (Life Sciences)
Skills Required
- Basic understanding of pharmacovigilance and AE reporting
- Knowledge of clinical research processes
- Good communication and documentation skills
- Proficiency in MS Office tools
- Attention to detail and organizational ability
Why This Role is High-Value (Career Perspective)
- Entry into pharmacovigilance domain (high growth field)
- Exposure to global safety databases and workflows
- Opportunity to work with a top CRO (IQVIA)
- Builds foundation for roles like:
- Drug Safety Associate
- PV Case Processor
- Safety Scientist
Benefits
- Structured learning in clinical safety & regulatory compliance
- Exposure to real-world AE case processing
- Career progression in clinical research and pharmacovigilance
- Opportunity to work in global projects and teams
How to Apply
