ICON plc, a global leader in clinical research and healthcare intelligence, is inviting applications for multiple roles โ CRA, CRA I, and CDC I โ 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.
๐ฌ 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:
- Bachelorโs 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:
- Bachelorโs 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.
๐ 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.
๐ How to Apply
Application Link For Senior CRA
