Clinical Research Associate II – ICON Strategic Solutions | Delhi & Bangalore
- Clinical Research Associate II – ICON PLC
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join ICON Strategic Solutions?
- FAQs
Clinical Research Associate II – ICON PLC
Apply for Clinical Research Associate II at ICON Strategic Solutions, Delhi & Bangalore. 3+ years CRA experience required. Global FSP opportunity!
ICON plc, a leading healthcare intelligence and clinical research organization, is inviting experienced professionals to join its Strategic Solutions (FSP/Client Dedicated Program) as a Clinical Research Associate II in Delhi or Bangalore. This position offers a chance to work with world-class experts in clinical research, advancing global healthcare through innovation, collaboration, and scientific excellence.
Company Overview
ICON Strategic Solutions, part of ICON plc, stands as a global leader in clinical development, providing end-to-end solutions that accelerate the delivery of life-changing therapies. With a focus on quality, integrity, and patient safety, ICON partners with leading pharmaceutical and biotech organizations worldwide. The company is known for its inclusive culture, continuous professional development opportunities, and strong emphasis on employee well-being.
ICON’s FSP (Functional Service Provider) model ensures that talented clinical professionals like you contribute directly to high-impact, client-dedicated programs while enjoying ICON’s supportive environment and career growth pathways.
Job Role & Responsibilities
As a Clinical Research Associate II (CRA II), you will play a pivotal role in managing and monitoring clinical trials to ensure accuracy, compliance, and safety. Your responsibilities will include:
- Conducting site qualification, initiation, monitoring, and close-out visits.
- Ensuring adherence to study protocols, GCP guidelines, and regulatory requirements.
- Verifying data accuracy and maintaining trial documentation integrity.
- Collaborating with investigators, site coordinators, and cross-functional teams to ensure smooth study execution.
- Reviewing case report forms (CRFs), resolving data discrepancies, and supporting clinical data management teams.
- Contributing to study start-up documentation and preparation of study reports.
This role demands strong analytical thinking, proactive problem-solving, and excellent communication skills to ensure project timelines and quality standards are consistently met.
Eligibility / Qualifications
To be considered for this role, candidates should meet the following criteria:
- Education: Bachelor’s degree in life sciences, pharmacy, biotechnology, nursing, or a healthcare-related field (e.g., B Pharm, MSc Life Sciences, BSc Nursing).
- Experience: Minimum 3 years of on-site clinical monitoring experience.
- Technical Knowledge: Strong understanding of ICH-GCP, clinical trial processes, and regulatory documentation.
- Skills: Excellent communication, data review, and organizational skills.
- Mobility: Willingness to travel for site monitoring visits as needed (via train, air, or car).
Location & Salary
- Work Location: Delhi or Bangalore (Office-based or Home-based depending on project allocation).
- Compensation: ICON offers a competitive salary and performance-linked incentives.
- Benefits: Health insurance, global employee assistance program, paid leave entitlements, life assurance, retirement planning, and flexible well-being programs.
Application Process
Interested candidates can apply directly through the official ICON careers portal:
👉 Apply Now
Why Join ICON Strategic Solutions?
- Work with a top-tier global CRO that partners with 90% of the world’s leading pharma companies.
- Be part of a diverse, inclusive, and innovation-driven culture.
- Access continuous learning programs and leadership pathways.
- Make a tangible impact on global healthcare outcomes.
FAQs
1. What is the minimum experience required for this role?
A minimum of 3 years of on-site monitoring experience as a CRA is required.
2. Can freshers apply for the CRA II position?
No, this position requires prior hands-on clinical trial monitoring experience.
3. What are the working conditions — remote or office-based?
Both options are available based on project and client requirements.
4. What benefits does ICON offer?
Comprehensive health insurance, paid time off, global EAP access, flexible benefits, and professional growth opportunities.
5. How can I apply?
Apply directly via ICON’s official career portal linked above.
Summary Table:
| Company | ICON Strategic Solutions (ICON plc) |
|---|---|
| Vacancies | Clinical Research Associate II |
| Required Education | BSc / MSc Life Sciences, B Pharm, Nursing, or related field |
| Experience | Minimum 3 years on-site clinical monitoring |
| Location | Delhi / Bangalore |
| Application Link | Apply Here |
To apply for this job please visit careers.iconplc.com.
