ICON Hiring Study Review Specialist: Chennai & Bangalore
Are you seeking rewarding clinical data review vacancies via ICON Careers India or Study Review Specialist Jobs? Global clinical research leader ICON is inviting applications for Study Review Specialists at its sites in Chennai and Bangalore.
This role requires 1 to 3 years of clinical trial operations experience, with mandatory hands-on experience reviewing study start-up document packages. To write an industry-aligned clinical documentation and GCP-compliant CV, read our guide on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | ICON Plc (ICON India Central Services) |
| Position | Study Review Specialist |
| Job Locations | Chennai (Tamil Nadu) & Bangalore (Karnataka) |
| Work Mode | Office with Flex |
| Employment Type | Full-Time |
| Experience Required | 1 – 3 Years in Clinical Research |
| Qualifications | Bachelor's Degree in Life Sciences or Related Field |
| Application Deadline | July 1, 2026 |
| Estimated Salary | ₹5.5 LPA – ₹8.5 LPA (Depending on profile) |
| Ref ID | JR148495 |
💼 Key Responsibilities
- Review and approve Critical Document Packages (CDPs) prior to Investigational Product (IP) release.
- Ensure complete compliance of files with sponsor SOPs, ICH-GCP principles, and local country regulations.
- Perform thorough reviews of study start-up documents for quality, accuracy, and compliance.
- Record and log all review activities, query management, and approvals inside ICON tracking databases.
- Meet strict CDP approval timelines and proactively escalate potential documentation delays.
- Perform internal parallel quality checks on TMF records and document packs.
- Collaborate actively with cross-functional global study teams and site startup coordinators.
- Act as a Subject Matter Expert (SME) for assigned document review and quality workflows.
- Mentor and coach new team members during onboarding and training sessions.
To learn how clinical operations and document specialist salaries scale compared to global pharmacovigilance pathways, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Experience
- Education: Bachelor’s degree in Life Sciences, Pharmacy (B.Pharm/M.Pharm), Doctor of Pharmacy (Pharm.D), or related disciplines.
- Experience: 1 to 3 years of clinical research experience, with specific exposure to study start-up, regulatory, or document review.
- Start-Up Focus: Hands-on experience reviewing study start-up documents (mandatory).
- Compliance: Strong understanding of ICH-GCP principles and regulatory documentation workflows.
- Skills: Meticulous attention to detail, strong communication skills, and proficiency with clinical tracking databases.
Preferred Skills:
- Prior experience in Contract Quality Control (QC).
- Exposure to Trial Master File (TMF) and Critical Document Package (CDP) evaluation.
For pharmacy postgraduates evaluating clinical trial documentation tracks versus lab research pathways, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join ICON?
- ICON is a premier award-winning global provider of outsourced development services to biopharma.
- Exposure to global clinical trials, advanced document management software, and international client projects.
- Comprehensive rewards packages, performance-related incentives, and flex-office options.
- Clear career pathways and structured professional training programs.
To test your knowledge of clinical trial protocols, data integrity, and GCP compliance terminology, take our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Study Review vs Healthcare IT
Study review specialists verify CDP folders and startup checklists for clinic trials, whereas healthcare IT professionals support backend server database setups. To understand these distinct careers, read our comparison on Healthcare IT vs Clinical Healthcare.
🚀 How to Apply?
Interested candidates should apply online directly on the official ICON Workday career portal. Click the button below to submit your application:
Apply Online - ICON Workday Portal❓ Frequently Asked Questions
Q. What is the required experience for this Study Review Specialist role?
ICON requires 1 to 3 years of clinical research experience, with mandatory exposure to study start-up document review.
Q. What is the work model and location?
This is a full-time, Office-with-Flex role based at ICON's Chennai or Bangalore offices.
Q. What is the application deadline?
The portal accepts applications until July 1, 2026.
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