Apply for CRA II Clinical Research Associate job at ICON plc India with clinical trial monitoring and global research exposure.
Are you an experienced Clinical Research professional looking to advance your career in global clinical trials? A new opportunity has opened for the CRA II – Clinical Research Associate II role across multiple Indian locations. This position offers strong career growth, international exposure, and the opportunity to work on innovative clinical development programs.
The CRA II position at ICON plc is ideal for candidates who already possess monitoring experience and want to contribute to cutting-edge clinical research studies while ensuring patient safety, regulatory compliance, and data integrity.
About ICON plc
ICON plc is a globally recognized healthcare intelligence and clinical research organization supporting pharmaceutical, biotechnology, and medical device companies worldwide. The organization delivers end-to-end clinical development solutions, helping bring innovative therapies and life-saving treatments to patients faster.
ICON is known for its inclusive culture, focus on innovation, and commitment to scientific excellence. Employees collaborate with global teams to design, manage, and analyze clinical trials across therapeutic areas.
Job Overview
Job Title: CRA II – Clinical Research Associate II
Job Locations:
- Bangalore
- Chennai
- Trivandrum
Work Mode: Office Based or Home Based
Job Type: Full Time
Job Requisition ID: JR147212
This role is designed for professionals with prior CRA experience who can independently manage study sites and ensure clinical trial success.
Role Summary
As a Clinical Research Associate II, you will act as a key link between sponsors, investigators, and clinical trial sites. The position focuses on monitoring clinical studies, maintaining regulatory compliance, ensuring patient safety, and verifying accurate clinical data collection.
You will contribute directly to clinical development programs that support the approval of new medicines and therapies worldwide.
Key Responsibilities
1. Clinical Trial Site Management
CRA II professionals are responsible for overseeing clinical trial activities at assigned study sites, including:
- Conducting Site Qualification Visits (SQV)
- Performing Site Initiation Visits (SIV)
- Monitoring clinical trial progress
- Completing Site Close-Out Visits
These activities ensure that clinical studies follow approved protocols and regulatory standards.
2. Protocol Compliance and Patient Safety
One of the most critical responsibilities of a CRA II includes:
- Ensuring study protocol adherence
- Monitoring patient safety standards
- Verifying informed consent procedures
- Maintaining Good Clinical Practice (GCP) compliance
Clinical Research Associates play a vital role in protecting trial participants.
3. Data Review and Query Resolution
The CRA II will:
- Review clinical trial data regularly
- Identify discrepancies or missing information
- Raise and resolve data queries
- Ensure data accuracy and reliability
High-quality clinical data is essential for regulatory submissions and drug approvals.
4. Collaboration with Investigators and Site Staff
Strong collaboration is essential for successful clinical trials. Responsibilities include:
- Coordinating with investigators and research coordinators
- Supporting site teams during study execution
- Providing training and guidance when required
- Maintaining effective communication with cross-functional teams
5. Study Documentation Support
The role also involves participation in clinical documentation processes such as:
- Reviewing study protocols
- Supporting clinical study reports
- Maintaining essential trial documents
- Ensuring audit readiness
Proper documentation ensures regulatory acceptance globally.
Required Qualifications
Candidates must meet the following educational and professional criteria:
Educational Qualification
- Bachelor’s degree in:
- Life Sciences
- Pharmacy
- Biotechnology
- Nursing
- Medical or Healthcare-related discipline
Experience Requirement
- Minimum 2 years of experience as a Clinical Research Associate
- Hands-on monitoring experience preferred
Technical Knowledge
Applicants should demonstrate:
- Strong understanding of clinical trial processes
- Knowledge of ICH-GCP guidelines
- Familiarity with global clinical regulations
- Experience with site monitoring activities
Key Skills
Successful candidates will possess:
- Excellent organizational abilities
- Strong communication skills
- Attention to detail
- Problem-solving capability
- Ability to work independently and within teams
Travel Requirement
This position requires approximately 60% travel, including:
- Domestic travel across study locations
- Possible international site visits
- Ability to travel by flight or road
A valid driver’s license is required for site visits.
Why Join ICON?
ICON focuses on building a supportive workplace that values professional growth, diversity, and employee well-being.
Career Advantages
Working at ICON provides:
- Exposure to global clinical trials
- Opportunity to work with innovative therapies
- International collaboration experience
- Structured career progression in clinical research
Employee Benefits
ICON offers a competitive compensation and benefits package designed to support employees and their families.
Benefits may include:
- Competitive salary packages
- Annual leave entitlements
- Comprehensive health insurance coverage
- Retirement planning programs
- Life insurance coverage
- Global Employee Assistance Programme support
- Flexible benefits depending on country policies
- Wellness programs and work-life balance initiatives
Work Culture and Inclusion
ICON promotes an inclusive and accessible work environment where diversity and belonging are fundamental values. The organization provides equal employment opportunities and maintains a workplace free from discrimination or harassment.
Employees are encouraged to apply even if they do not meet every listed requirement, as ICON values potential, passion, and growth mindset.
Who Should Apply?
This role is best suited for:
- Experienced Clinical Research Associates
- Professionals currently working in CROs
- Candidates seeking global clinical trial exposure
- Clinical research professionals looking for career advancement
- Healthcare or life sciences graduates with monitoring experience
Career Growth Opportunities
After gaining experience as a CRA II, professionals may progress into roles such as:
- Senior Clinical Research Associate
- Lead CRA
- Clinical Trial Manager
- Clinical Operations Manager
- Project Manager – Clinical Research
ICON’s global network provides long-term career development opportunities within clinical development and healthcare intelligence.
How to Apply
Interested candidates can apply online by following these steps:
- Visit the official ICON Careers website.
- Search using Job Requisition ID: JR147212.
- Select preferred location (Bangalore, Chennai, or Trivandrum).
- Choose Office-Based or Home-Based option.
- Click Apply and create your candidate profile.
- Upload updated resume highlighting CRA monitoring experience.
- Submit the application and wait for recruiter communication.
