PHARMAFull-time
Centralized Site Associate
THANE (IN)ONSITEPOSTED: 7/17/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
ROLE DEFINITION & RESPONSIBILITIES
Key Responsibilities
Perform centralized monitoring activities
Review site quality and protocol compliance
Monitor pending queries and SDV backlog
Support Clinical Trial Management teams
Review subject-level clinical data
Perform clinical trend analysis
Maintain CTMS, EDC and IXRS systems
Review inclusion/exclusion criteria
Review adverse events and SAEs
Generate study analytics
Identify operational risks
Recommend monitoring actions
Support study compliance
Assist in automation using Excel macros
Act as backup for Centralized Monitors
Eligibility
Graduate/Postgraduate degree in Life Sciences
2–5 years experience
Minimum 1 year relevant Clinical Research experience
Knowledge of: Electronic Data Capture (EDC), CTMS, IXRS, ICH-GCP, Clinical Trial Operations, Clinical Data Review, Global Clinical Trials
Strong Microsoft Excel skills
Excellent communication skills
Good analytical abilities
REQUIRED VERIFIED SKILLS
Electronic Data Capture (EDC)
CTMS
IXRS
ICH-GCP
Clinical Trial Operations
Clinical Data Review
Global Clinical Trials
Microsoft Excel
COMPENSATION & REWARDS
₹7.0L - 11.0L per annum
The estimated annual salary for this position is between ₹7 and ₹11 LPA, aligning with industry benchmarks for experienced clinical research professionals. Final compensation varies based on specific skills, background, and interview evaluations.
ORGANIZATION CONTEXT & CULTURE
IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services (CRO) to the life sciences industry. The company helps pharmaceutical, biotech, and medical device clients accelerate the development and commercialization of new medical treatments through its extensive data, technology, and human expertise. Their offerings span from clinical trial design and execution to real-world evidence and commercial effectiveness.
TEAM SIZE: 87,000+ employees
INDUSTRY: Healthcare Technology & Contract Research
EXPECTED CAREER ROADMAP
As a global leader in clinical research, IQVIA provides a robust framework for career advancement. Associates gain deep insights into data review and risk-based monitoring, allowing them to transition into senior clinical monitoring or operational management roles.
APPLICATION ADVISORY
Focus on highlighting your direct experience with EDC, CTMS, and clinical data review. Mentioning specific experience with Excel macros or automation, along with strong analytical skills during trend analysis discussions, will significantly boost your profile.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.