ICON plc, a global leader in clinical research and healthcare intelligence, is inviting applications for multiple roles — CRA, CRA I, and CDC I — in Bangalore, Chennai, and Trivandrum.
These positions are ideal for life sciences graduates passionate about advancing clinical development and ensuring regulatory excellence in global healthcare trials.
🔬 Available Positions
1. Senior Clinical Research Associate (CRA)
Location: Bangalore | Remote: Yes | Job ID: JR136767
As a Senior CRA, you will oversee clinical trial sites, ensuring adherence to ICH-GCP, regulatory protocols, and participant safety.
Key Responsibilities:
- Monitor and manage clinical trial sites.
- Ensure compliance with study protocols and data integrity.
- Conduct site visits and resolve issues promptly.
- Train and support site staff and junior CRAs.
- Collaborate with cross-functional global teams.
Qualifications:
- Advanced degree in Life Sciences, Medicine, or Nursing.
- Extensive CRA experience with regulatory and GCP knowledge.
- Strong site management, analytical, and interpersonal skills.
- Willingness to travel (up to 60%).
2. Clinical Research Associate I (CRA I)
Location: Bangalore | Remote/Office: Hybrid | Job ID: JR135687
The CRA I role involves managing clinical trial activities from setup to close-out, ensuring compliance with all study and safety protocols.
Key Responsibilities:
- Coordinate and monitor study activities.
- Maintain accurate site documentation.
- Review data and resolve sponsor queries.
- Build strong relationships with investigators and site staff.
Qualifications:
- Bachelor’s degree in Medicine, Pharmacy, or Life Sciences.
- Strong grasp of ICH-GCP and clinical data review.
- Excellent communication and report-writing skills.
- Travel flexibility (up to 60%).
3. Clinical Data Coordinator I (CDC I)
Location: Bangalore / Chennai / Trivandrum | Remote: Hybrid | Job ID: JR136690
The CDC I will manage clinical data collection and analysis, supporting data integrity and study timelines.
Key Responsibilities:
- Develop eCRF and data validation specifications.
- Review and clean data per study protocols.
- Generate and track data queries.
- Collaborate with data management and clinical teams.
Qualifications:
- Bachelor’s in Life Sciences, Biotech, or Healthcare.
- Knowledge of Medidata/Oracle RDC preferred.
- Strong analytical and detail-oriented mindset.
- Familiarity with ICH-GCP and data standards.
🎁 Benefits of Working at ICON plc
ICON offers a competitive salary and a comprehensive benefits package, including:
- Annual leave and flexible work options.
- Health insurance for you and your family.
- Retirement and savings plans.
- Employee wellness and assistance programs (TELUS Health).
- Optional perks like gym memberships, travel subsidies, and health assessments.
📝 How to Apply
Application Link For Senior CRA
