IQVIA Hiring Centralized Monitoring Assistant

IQVIA Hiring Centralized Monitoring Assistant | Freshers + Experience

Mohit April 30, 2026

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✔ Verified by Medical Jobs India

Hiring Centralized Monitoring Assistant

🏢 IQVIA

📍 Pune & Thane

🎓 Life Sciences

📊 RBM / Monitoring

IQVIA is hiring Centralized Monitoring Assistant for clinical trial monitoring and analytics roles. Strong opportunity for freshers + 6 months experience candidates in clinical research.

👉 Start clinical career: Clinical Research Guide

📋 Job Overview

Role: Centralized Monitoring Assistant
Company: IQVIA
Location: Pune & Thane
Experience: 6 Months – 2 Years
Job Type: Full-Time

🚀 Key Responsibilities

Support clinical study teams
Prepare trackers, reports & dashboards
Monitor KRIs & site performance
Identify risks and issues
Recommend CAPA actions
Support documentation & site packs
Participate in meetings & updates
Ensure ICH-GCP compliance

📘 Learn RBM: Clinical Data vs Monitoring Guide

🎓 Eligibility & Qualifications

B.Pharm / M.Pharm / BSc / MSc
0–2 years experience
Basic ICH-GCP knowledge
MS Excel & reporting skills
Strong communication skills

🎯 Practice: Clinical Quiz

💻 Key Skills

Risk-Based Monitoring (RBM)
Clinical data analysis
Dashboard & reporting
Attention to detail
Stakeholder coordination

💰 Salary & Benefits

₹4.5 – ₹7.5 LPA
Global trial exposure
Career growth in clinical operations
Advanced analytics learning

🚀 Career Growth

Clinical Data Manager
Clinical Research Associate (CRA)
Risk-Based Monitoring Specialist
Clinical Project Manager

💡 Interview Tips

Understand RBM concept
Revise GCP guidelines
Prepare KRI examples
Focus on data interpretation

📄 Resume Tips

Mention clinical exposure
Add Excel/reporting skills
Use keywords: RBM, GCP, CRO
Keep resume 1–2 pages

❓ FAQ

Freshers eligible? ✔ Yes
Experience required? 0–2 years
Domain? Clinical Monitoring

🚀 Job Application Link

⏰ Last Date to Apply: 2 May 2026

🚀 Apply Now: Centralized Monitoring Assistant (IQVIA)

📌 Important Note Before You Apply:

Kindly read the job description carefully before applying. Ensure your profile aligns with centralized clinical trial monitoring, data review, and site support requirements before proceeding.