Clinical Research Associate II Position at ICON in Bangalore
An ICON Clinical Research opportunity in Bangalore has emerged for experienced professionals in clinical research. ICON plc, a globally recognized Clinical Research Organization (CRO), is seeking a Clinical Research Associate II (CRA II) in Bangalore, India. This opportunity is tailored for individuals with over 2 years of CRA experience who aspire to contribute to global clinical trials, patient safety, and regulatory compliance.
About the Company
ICON plc is a leading global provider of outsourced development and commercialization services to the pharmaceutical, biotechnology, and medical device industries. Headquartered in Dublin, Ireland, ICON operates in various locations worldwide, including Bangalore, India. The organization is committed to delivering high-quality clinical research services and innovative solutions to its clients, ensuring the advancement of medical science and patient care.
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 a CRA
ICON Clinical Research Bangalore: Job Description
As a CRA II at ICON, the selected candidate will manage clinical trial sites while ensuring adherence to regulatory compliance. This role involves conducting various site visits, ensuring ICH-GCP compliance, and collaborating with site staff and sponsors to support clinical trial documentation.
Key Responsibilities
- 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 Criteria
- Bachelor’s degree in Life Sciences / Pharmacy / Healthcare.
- Minimum 2 years of CRA experience.
- Strong understanding of ICH-GCP guidelines, clinical trial lifecycle, and 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 Salary: ₹6.5 LPA – ₹12 LPA (based on experience, CRO standards, and travel requirements).
Benefits at ICON
ICON offers competitive and employee-focused benefits, including:
- 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 a CRA II at ICON Role Is Important for Your Career
This Clinical Research Associate II role at ICON is ideal for those looking to transition into global CRO operations, strengthen expertise in clinical monitoring and GCP compliance, work on multi-country clinical trials, and build a long-term career in clinical research, pharmacovigilance, or regulatory affairs.
How to Apply
Conclusion
The CRA II at ICON opportunity presents an excellent pathway for qualified candidates to advance their careers in clinical research. Interested individuals are encouraged to apply at the earliest to seize this chance for professional growth.
