Looking to advance your career in clinical research? ICON plc, a globally recognized Clinical Research Organization (CRO), is hiring a Clinical Research Associate II (CRA II) in Bangalore, India. This is an excellent opportunity for professionals with 2+ years of CRA experience who want to work on global clinical trials, patient safety, and regulatory compliance.
If you’re aiming to grow in clinical trial monitoring, GCP compliance, and site management, this role offers strong exposure to international studies and cutting-edge therapies.
Job Details
- Position: Clinical Research Associate II
- Company: ICON plc
- Location: Bangalore, India
- Mode: Office / Home (Hybrid/Remote flexibility)
- Job Type: Full-time
- Experience: Minimum 2 years as CRA
- Application Deadline: 18 March 2026
Key Responsibilities (Clinical Research Associate II)
As a CRA II at ICON, you will be responsible for managing clinical trial sites and ensuring regulatory compliance:
- Conduct Site Qualification Visits (SQV), Site Initiation Visits (SIV), Monitoring Visits (MV), and Close-Out Visits (COV)
- Ensure ICH-GCP compliance, protocol adherence, and patient safety
- Perform clinical data review, query resolution, and data validation
- Collaborate with investigators, site staff, and sponsors
- Support clinical trial documentation, including protocols and Clinical Study Reports (CSR)
- Maintain data integrity and audit readiness
Eligibility & Qualifications
To apply for this Clinical Research Associate II job, candidates should have:
- Bachelorโs degree in Life Sciences / Pharmacy / Healthcare
- Minimum 2 years of CRA experience
- Strong understanding of:
- ICH-GCP guidelines
- Clinical trial lifecycle
- Regulatory requirements
- Excellent communication, organizational, and monitoring skills
- Ability to work independently and in cross-functional teams
- Willingness to travel up to 60% (domestic & international)
Salary (Estimated for CRA II in India)
- โน6.5 LPA โ โน12 LPA (based on experience, CRO standards, and travel requirements)
Benefits at ICON
ICON offers competitive and employee-focused benefits:
- Comprehensive health insurance
- Annual leave & work-life balance policies
- Retirement planning benefits
- Global Employee Assistance Programme (TELUS Health)
- Life insurance coverage
- Flexible benefits (gym membership, travel support, childcare options)
- Opportunity to work on global clinical trials
Why This Role is Important for Your Career
This Clinical Research Associate II role at ICON is ideal if you want to:
- Transition into global CRO operations
- Strengthen expertise in clinical monitoring & GCP compliance
- Work on multi-country clinical trials
- Build a long-term career in clinical research, pharmacovigilance, or regulatory affairs
How to Apply
