If you’re looking for Study Review Specialist Jobs in India, ICON is hiring talented clinical research professionals for its offices in Chennai and Bangalore. This opportunity is ideal for candidates with 1-3 years of experience in study start-up document review, clinical document management, regulatory operations, or clinical research.
Professionals with a background in Life Sciences and hands-on experience reviewing study start-up documents and clinical trial documentation are encouraged to apply.
Job Details
| Particular | Details |
|---|---|
| Company | ICON |
| Position | Study Review Specialist |
| Job Type | Full-Time |
| Work Mode | Office with Flex |
| Location | Chennai, Bangalore |
| Experience | 1โ3 Years |
| Qualification | Bachelor’s Degree in Life Sciences or Related Field |
| Industry | Clinical Research / CRO |
| Application Deadline | July 1, 2026 |
About ICON
ICON is a global healthcare intelligence and clinical research organization dedicated to helping bring innovative medicines and treatments to patients faster. The company partners with pharmaceutical, biotechnology, and medical device organizations worldwide while maintaining high standards of quality, regulatory compliance, and patient safety.
Key Responsibilities
As a Study Review Specialist, you will:
- Review and approve Critical Document Packages (CDPs) before Investigational Product release.
- Ensure compliance with ICH-GCP guidelines, sponsor SOPs, and regulatory requirements.
- Review study start-up documentation for completeness and quality.
- Maintain documentation and tracking activities within ICON systems.
- Ensure document review timelines are achieved.
- Perform internal quality reviews of Trial Master File (TMF) documentation.
- Collaborate with study teams and cross-functional departments.
- Participate in study meetings and documentation reviews.
- Support process improvement initiatives.
- Mentor new team members during onboarding.
- Act as Subject Matter Expert (SME) for assigned document review processes.
Eligibility Criteria
Applicants should have:
- Bachelor’s degree in Life Sciences or a related discipline.
- 1-3 years of experience in Clinical Research.
- Hands-on experience reviewing Study Start-up Documents (mandatory).
- Experience in Contract Quality Control (preferred).
- Knowledge of ICH-GCP guidelines.
- Understanding of regulatory documentation.
- Experience with clinical documentation systems.
- Excellent attention to detail.
- Good communication and collaboration skills.
Preferred Skills
- Clinical Trial Documentation
- Study Start-Up
- Regulatory Documentation
- Trial Master File (TMF)
- Critical Document Package (CDP)
- Clinical Operations
- Quality Review
- Clinical Compliance
- Documentation Review
- Stakeholder Communication
Salary (Estimated)
Based on similar Clinical Research opportunities in India:
โน5.5 LPA โ โน8.5 LPA
Actual compensation depends on experience, skills, and interview performance.
Employee Benefits
ICON offers:
- Competitive salary
- Performance incentives
- Medical insurance
- Dental and vision benefits (where applicable)
- Retirement and pension plans
- Life insurance
- Employee assistance programs
- Learning and development programs
- Career growth opportunities
- Flexible work environment
Why Join ICON?
ICON is one of the world’s leading Clinical Research Organizations (CROs), offering professionals exposure to global clinical trials, regulatory operations, quality management, and advanced clinical technologies. Employees benefit from structured career progression and continuous learning in an international work environment.
How to Apply
