Looking to start your career in Pharmacovigilance and Drug Safety? Here’s an exciting opportunity to join one of the world’s leading clinical research organizations, IQVIA, as an Operations Coordinator 1.
If you are a B.Pharm, M.Pharm, or Diploma in Pharmacy graduate eager to build your future in Lifecycle Safety and Case Processing, this could be the perfect entry-level role for you. 💊📊
🏢 About IQVIA
IQVIA is a globally recognized clinical research and healthcare intelligence organization known for advancing healthcare through data-driven insights and innovative technologies.
With operations across multiple countries, IQVIA plays a critical role in:
- Clinical Trials
- Pharmacovigilance
- Regulatory Support
- Real-World Evidence Solutions
This position is part of their Lifecycle Safety team, focusing on Adverse Event (AE) management and safety case processing.
📌 Job Overview
- Job Title: Operations Coordinator 1
- Location: Kochi / Kolkata
- Experience: 0 Years (Freshers Eligible)
- Openings: 10 Vacancies
- Industry: Clinical Research / CRO
- Employment Type: Full-Time, Permanent
If you are passionate about drug safety, regulatory compliance, and patient safety monitoring, this role offers hands-on exposure to real-world pharmacovigilance operations. 🌍
🎯 Key Responsibilities
🧾 1. Adverse Event (AE) & Case Processing Support
- Collecting and tracking incoming Adverse Events (AE)
- Identifying initial and follow-up cases
- Tracking case processing timelines
- Distributing case data to project teams
- Transferring safety events to clients
- Ensuring submission acknowledgment and confirmation
🗂️ 2. Database & Documentation Activities
- Database entry and quality checks
- Assisting in Lifecycle Safety reports
- Supporting safety submission dossiers
- Creating project-specific entry specifications
- Assisting in User Acceptance Testing (UAT)
- Performing ad hoc database searches
📦 3. Project & Administrative Support
- Maintaining project files
- Managing system access requests
- Preparing AE listings
- Shipping safety documentation to sites
- Coordinating meetings
- Handling courier dispatch and stationery orders
📁 4. Records & Archiving Management
- Creating and maintaining case folders
- Filing and retrieving documentation
- Archiving safety files after case closure
- Supporting records transfer to archive facilities
- Assisting in improving records management processes
👩🏫 5. Training & Continuous Improvement
- Mentoring junior team members
- Identifying process improvements
- Participating in departmental committees
- Reporting quality issues to senior staff
This role provides structured exposure to:
- ICSR processing
- Argus Safety Database
- Global safety reporting workflows 📈
🛠️ Required Skills
✅ Must-Have Knowledge
- Drug Safety basics
- Lifecycle Safety data processing
- Case Processing
- ICSR handling
- Argus (Preferred but not mandatory for freshers)
🎓 Educational Qualification
- B.Pharm
- M.Pharm
- Diploma in Pharmacy
Fresh graduates interested in Pharmacovigilance, Regulatory Affairs, or Clinical Research are highly encouraged to apply.
🌟 Why This Role is a Great Start for Freshers
Starting your career in Pharmacovigilance can open multiple growth paths:
- Drug Safety Associate
- Pharmacovigilance Executive
- Medical Reviewer
- Safety Database Specialist
- Regulatory Affairs Professional
Working with IQVIA allows you to gain international exposure to safety reporting standards and global pharmaceutical compliance systems. 🌍
💡 Career Growth Opportunities
After 1–2 years of experience, professionals often move into:
- Senior Case Processing roles
- Safety Team Lead positions
- Signal Detection & Risk Management
- Aggregate Report Writing
- Regulatory Submissions Management
The Pharmacovigilance sector continues to grow rapidly due to increasing global regulatory requirements. 📊
🧠 Who Should Apply?
✔️ Pharmacy freshers looking for entry-level PV jobs
✔️ Candidates interested in Adverse Event reporting
✔️ Graduates targeting Clinical Research careers
✔️ Individuals comfortable with documentation & databases
✔️ Candidates willing to relocate to Kochi or Kolkata
📍 Work Locations
- Kochi
- Kolkata
Both cities are emerging hubs for CRO and pharmacovigilance operations in India. 🏙️
📢 Resume Tips (Important for Freshers)
Since you’re starting out, make sure your resume highlights:
- Knowledge of ICH-GCP guidelines
- Basic understanding of Adverse Event reporting
- Any internship in Clinical Research or Drug Safety
- Familiarity with safety databases (if applicable)
- Strong documentation and communication skills
Given your writing background and strong academic foundation, crafting a keyword-optimized resume can significantly increase your shortlisting chances—especially for ATS screening.
🚀 Final Thoughts
Entry-level Drug Safety roles like this are highly competitive due to the growing demand in the pharmaceutical and CRO industry.
If you’re serious about building a long-term career in Pharmacovigilance and Clinical Research, this opportunity at IQVIA could be your gateway into the global drug safety ecosystem. 💊🌍
Apply here:
👉 https://www.linkedin.com/redir/redirect/?url=http%3A%2F%2Fnauk%2Ein%2Fchoymdu&urlhash=_V1X&isSdui=true
