Clinical Research Associate II – ICON Strategic Solutions | Bangalore
- ICON Hiring CRA II in India | Remote Clinical Research Associate Jobs 2026
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Eligibility / Qualifications
- Educational Qualification:
- Relevant Courses:
- Experience:
- Skills Required:
- Location & Salary
- Job Location:
- Salary:
- Benefits:
- Application Process
- Why This Role Matters
- Frequently Asked Questions (FAQs)
- 1. Is this role remote?
- 2. What experience is required?
- 3. What qualifications are needed?
- 4. Is travel mandatory?
- 5. What type of company is ICON?
- Summary
ICON Hiring CRA II in India | Remote Clinical Research Associate Jobs 2026
ICON plc is actively hiring for the position of Clinical Research Associate II (CRA II) in India. This opportunity is open to experienced clinical research professionals looking to work in a global CRO environment with flexible remote working and travel opportunities.
This hiring is for the Clinical Monitoring department, offering a high-growth role for candidates with at least 2 years of CRA experience. The position is primarily remote but requires frequent travel for on-site monitoring visits across India and potentially internationally.
Company Overview
ICON plc is a globally recognized clinical research organization (CRO) specializing in healthcare intelligence, clinical development, and data-driven solutions. With operations across multiple countries, ICON supports pharmaceutical, biotechnology, and medical device companies in bringing innovative therapies to market.
The company is known for its strong focus on clinical trial excellence, regulatory compliance, and patient safety. ICON provides end-to-end clinical research services, making it a preferred employer for professionals in pharmacovigilance, clinical operations, and regulatory affairs.
Working at ICON offers exposure to multinational clinical trials, advanced clinical systems, and global regulatory frameworks.
Job Role & Responsibilities
As a Clinical Research Associate II, you will be responsible for managing clinical trial sites and ensuring high-quality study execution.
Key Responsibilities:
- Conduct site qualification, initiation, monitoring, and close-out visits
- Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements
- Monitor patient safety and maintain data integrity throughout clinical trials
- Review clinical data and resolve queries in collaboration with site teams
- Coordinate with investigators, sponsors, and cross-functional teams
- Support preparation and review of clinical trial documentation and reports
- Maintain accurate trial records in systems such as CTMS and eTMF
This role plays a critical part in ensuring that clinical trials meet global regulatory standards and deliver reliable results.
Eligibility / Qualifications
Educational Qualification:
- Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field
Relevant Courses:
B.Pharm, M.Pharm, Pharm.D, B.Sc Life Sciences, M.Sc Clinical Research, Biotechnology, Microbiology, Biochemistry, Nursing, Clinical Data Management
Experience:
- Minimum 2 years of experience as a Clinical Research Associate
- Strong hands-on experience in site monitoring visits (8–9 visits/month)
Skills Required:
- Strong understanding of clinical trial processes and ICH-GCP guidelines
- Excellent communication and stakeholder management skills
- Ability to manage multiple sites and timelines effectively
- Strong analytical and problem-solving capabilities
- Willingness to travel up to 60%
Location & Salary
Job Location:
- Remote (India) with travel requirements
Salary:
- Competitive salary package with performance-based benefits
Benefits:
- Health insurance and wellness programs
- Retirement and financial planning support
- Paid leaves and work-life balance initiatives
- Employee assistance programs and global support services
Application Process
Candidates can apply directly through the official ICON careers page:
Apply Here: https://careers.iconplc.com/job/cra-ii-in-india-bangalore-jid-49292
Candidates are encouraged to apply early due to high demand for CRA roles in the clinical research industry.
Why This Role Matters
Clinical Research Associates are at the core of drug development and clinical trial execution. This role ensures that new therapies are tested ethically, efficiently, and in compliance with global standards.
Joining ICON allows professionals to work on international clinical trials, gain exposure to cutting-edge research, and contribute directly to advancing healthcare outcomes.
Frequently Asked Questions (FAQs)
1. Is this role remote?
Yes, but it requires travel for on-site monitoring visits.
2. What experience is required?
Minimum 2 years as a CRA.
3. What qualifications are needed?
Life sciences, pharmacy, or healthcare-related degree.
4. Is travel mandatory?
Yes, up to 60% travel is required.
5. What type of company is ICON?
ICON is a global clinical research organization (CRO).
Summary
| Category | Details |
|---|---|
| Company | ICON plc |
| Vacancies | Clinical Research Associate II |
| Required Education | B.Pharm, Life Sciences |
| Experience | Minimum 2 Years |
To apply for this job please visit careers.iconplc.com.
