Senior Clinical Research Associate (Senior CRA) – Phase IV / PMS / RWE | Bangalore, India
Job ID: JR144469
Location: Bangalore, India (Office-Based, Non-Flexible)
Employment Type: Full-Time
Application Deadline: February 28, 2026
Company: ICON plc
About ICON plc
ICON plc is a leading global contract research organization (CRO) delivering clinical development and healthcare intelligence solutions to pharmaceutical, biotechnology, and medical device companies. With a strong global footprint, ICON supports end-to-end clinical trial execution across all phases, including post-marketing and real-world evidence programs.
Position Overview
ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CRA) to support Phase IV, Post-Marketing Surveillance (PMS), and Real-World Evidence (RWE) studies in Bangalore. This office-based role requires strong site monitoring expertise, regulatory knowledge, and the ability to independently manage multiple clinical studies.
The Senior CRA will play a critical role in ensuring protocol compliance, data integrity, participant safety, and adherence to ICH-GCP and regulatory standards throughout the study lifecycle.
Experience Required
Minimum 5+ years of overall experience in clinical research.
At least 2–3 years of independent CRA/site monitoring experience.
Mandatory experience in Phase II–IV studies.
Proven exposure to PMS (Post-Marketing Surveillance) and Real-World Evidence (RWE) studies.
Key Responsibilities
Conduct site monitoring visits (SIV, IMV, COV) to ensure compliance with study protocols, regulatory guidelines, and Good Clinical Practice (GCP).
Oversee Phase IV, PMS, and RWE clinical trial activities, ensuring quality and accuracy of collected data.
Review essential documents, source data verification (SDV), and maintain inspection readiness.
Identify, escalate, and resolve site performance or compliance issues.
Collaborate with cross-functional teams including Medical, Data Management, Regulatory, and external CRO partners.
Provide training and support to site staff and junior CRAs when required.
Manage multiple studies independently while meeting project timelines and deliverables.
Required Qualifications & Skills
Strong knowledge of ICH-GCP, regulatory requirements, and post-marketing study frameworks.
Experience working with CROs, vendors, and cross-functional medical teams.
Excellent documentation, administrative, and reporting skills.
Strong stakeholder management and communication abilities.
High level of organizational skills and ability to manage concurrent projects.
Core Keywords for SEO Optimization
Senior CRA Jobs India, Clinical Research Associate Bangalore, Phase IV Clinical Trials, Post-Marketing Surveillance Jobs, Real-World Evidence Studies, CRO Careers India, ICH-GCP Monitoring, Clinical Trial Monitoring Jobs.
Why Join ICON plc
ICON offers competitive compensation and a comprehensive benefits package designed to support employee well-being and professional growth, including:
Annual leave entitlements
Health insurance coverage
Retirement savings plans
Life assurance
Global Employee Assistance Programme (TELUS Health)
Flexible, country-specific optional benefits
ICON is committed to diversity, inclusion, and equal opportunity employment, ensuring a professional environment free from discrimination and harassment.
How to Apply
Qualified Clinical Research Associates with strong Phase IV, PMS, and RWE monitoring experience are encouraged to apply through the official ICON careers portal before the application deadline.
For more global Clinical Research, CRA, and CRO job opportunities, visit ThePharmaDaily.com.
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