Central Report Reviewer (CRR)
Company: Syneos Health
Location: Remote (India)
Job ID: 25109861
Updated On: June 29, 2026
Job Summary
Syneos Health is hiring a Central Report Reviewer (CRR) to independently review and approve Phase I–IV clinical trial monitoring reports, ensuring compliance with study protocols, ICH-GCP, regulatory requirements, patient safety, and data integrity. The role involves reviewing site and central monitoring documentation, identifying compliance risks, supporting monitoring teams, and collaborating with Clinical Trial Managers (CTMs), Clinical Research Associates (CRAs), and project teams to maintain high-quality clinical trial execution.
Key Responsibilities
Execute Central Report Review (CRR) activities for assigned clinical studies.
Review and approve site monitoring and central monitoring reports.
Ensure compliance with study protocols, ICH-GCP, SOPs, and regulatory guidelines.
Assess patient safety, protocol compliance, and clinical data integrity.
Support the development of annotated visit reports such as PSV, SIV, IMV, COV, and SCAN.
Review site visit reports, monitoring calls, site letters, and project correspondence.
Verify the quality and completeness of monitoring documentation.
Document report revisions, approvals, and maintain records in CTMS.
Identify protocol deviations, GCP violations, and pharmacovigilance concerns.
Escalate critical compliance and patient safety issues to Clinical Trial Managers (CTMs) and Project Managers.
Record observations and ensure action items are assigned to CRAs or relevant teams.
Assess CRA and Clinical Monitor report quality, risks, and operational trends.
Prepare findings and summaries for CTM review and action planning.
Participate in project meetings, clinical training sessions, and cross-functional discussions.
Maintain up-to-date project knowledge through regular communication and documentation review.
Required Skills
Central Report Review (CRR)
Clinical Monitoring
Clinical Trial Management
Clinical Operations
ICH-GCP Compliance
Regulatory Compliance
Site Monitoring Reports
Central Monitoring Reports
CTMS (Clinical Trial Management System)
Protocol Compliance
Protocol Deviation Management
Patient Safety
Clinical Data Integrity
Risk Assessment
Pharmacovigilance Awareness
Quality Review
Analytical Thinking
Documentation Review
Communication & Collaboration
Attention to Detail
Eligibility
Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or another healthcare-related discipline.
Experience in Clinical Research, Clinical Monitoring, or Clinical Operations is preferred.
Good understanding of Phase I–IV clinical trials, ICH-GCP, and applicable regulatory requirements.
Strong analytical, documentation, and communication skills.
Experience
Preferred Experience: 3–5 years of experience in Clinical Monitoring, CRA, Central Monitoring, Clinical Operations, Clinical Quality Review, or Clinical Trial Management.
Salary Package (Estimated Market Standard)
₹8 LPA – ₹12 LPA (depending on experience, clinical monitoring expertise, and interview performance).
Work Mode
Remote (India)
Why Join Syneos Health?
Fully remote opportunity with exposure to global clinical trials.
Work on Phase I–IV studies with international sponsors.
Continuous learning, career development, and technical training.
Inclusive and collaborative work culture.
Employee recognition and performance-based rewards.
Opportunity to contribute to patient safety and clinical research quality on a global scale.
About Syneos Health
Syneos Health is a leading global life sciences organization that partners with pharmaceutical, biotechnology, and healthcare companies throughout the drug development and commercialization lifecycle. Over the past five years, the company has contributed to 94% of FDA-approved novel drugs, 95% of EMA-authorized products, and supported 200+ clinical studies across 73,000 sites involving more than 675,000 clinical trial participants.
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Remote, India | Siliguri |Illinois :
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Bangor | Brewer |New Jersey :
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Canada |Quebec :
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Brussels |Antwerp :
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Zaventem |South America :
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Brazil | Sao paulo |Attica :
Koropi | Athens |Greece :
Greece |North Island :
Auckland |New Zealand :
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Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
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Japan | Saitama |Tokyo :
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Niš |Bohemia :
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Santiago |Bosnia and Herzegovina :
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