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Site Visit Report Reviewer

Parexel
3-8 years
INR 9 LPA – 16 LPA
Remote
1 June 18, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes

Site Visit Report Reviewer (SVRR)

Department: Clinical Operations
Location: Remote – India
Company: Parexel
Reporting To: Clinical Operations Leader (COL) / Clinical Operations Management
Experience: 3–8 Years
Education: Life Sciences / Pharmacy / Nursing / Healthcare Degree


Role Summary

The Site Visit Report Reviewer (SVRR) is responsible for ensuring the quality, accuracy, completeness, and regulatory compliance of site monitoring documentation generated during clinical trials. The role serves as a quality oversight function supporting Clinical Research Associates (CRAs), Clinical Operations Leaders (COLs), and project teams by reviewing monitoring visit reports, tracking site issues, and ensuring adherence to protocol requirements, ICH-GCP guidelines, sponsor expectations, and company SOPs.

The SVRR contributes significantly to inspection readiness, risk identification, and overall study quality by ensuring timely resolution of monitoring findings and study-related issues.


Key Responsibilities

1. Monitoring Visit Report Review

  • Review and approve:

    • Site Qualification Visit Reports (SQV)

    • Site Initiation Visit Reports (SIV)

    • Routine Monitoring Visit Reports (MVR)

    • Close-Out Visit Reports (COV)

  • Verify completeness, consistency, and quality of monitoring documentation.

  • Ensure reports accurately reflect site activities and protocol compliance.

  • Review reports within established turnaround timelines.


2. Quality & Compliance Oversight

  • Ensure compliance with:

    • ICH-GCP Guidelines

    • Applicable Regulatory Requirements

    • Sponsor Requirements

    • Parexel SOPs and Work Instructions

  • Identify documentation deficiencies, inconsistencies, and compliance risks.

  • Escalate critical issues to Clinical Operations Leaders and project teams.

  • Support inspection and audit readiness activities.


3. Issue Tracking & Follow-Up

  • Monitor and track:

    • Open Action Items

    • Protocol Deviations (PDs)

    • Serious Adverse Events (SAEs)

    • Corrective and Preventive Actions (CAPAs)

  • Ensure timely closure of outstanding site issues.

  • Collaborate with CRAs to obtain clarifications and corrective actions.

  • Maintain accurate tracking logs and issue management reports.


4. Clinical Trial Quality Management

  • Perform trend analysis of monitoring findings.

  • Identify recurring quality concerns across sites and studies.

  • Recommend process improvements to enhance monitoring quality.

  • Support risk-based monitoring strategies through data review and analysis.


5. Stakeholder Collaboration

  • Work closely with:

    • Clinical Research Associates (CRAs)

    • Clinical Operations Leaders (COLs)

    • Project Managers

    • Quality Assurance Teams

    • Sponsors

  • Participate in study meetings and quality review discussions.

  • Provide guidance regarding monitoring documentation requirements.


6. Metrics, Reporting & Continuous Improvement

  • Generate periodic quality review reports.

  • Analyze monitoring visit trends and quality metrics.

  • Contribute to process optimization initiatives.

  • Support development of best practices and training materials.


Key Performance Indicators (KPIs)

  • Monitoring report review turnaround time

  • Quality review accuracy

  • Protocol deviation tracking and closure

  • SAE follow-up completion

  • Audit and inspection readiness

  • Compliance with SOP timelines

  • Stakeholder satisfaction

  • Quality trend analysis outputs


Required Qualifications

Education

  • Bachelor's Degree in:

    • Life Sciences

    • Pharmacy

    • Nursing

    • Biotechnology

    • Medical Sciences

  • Advanced Clinical Research Certification preferred


Experience

  • 3–8 years in Clinical Research

  • Experience as:

    • Clinical Research Associate (CRA)

    • Senior CRA

    • Clinical Trial Coordinator

    • Site Management Associate

    • Clinical Quality Reviewer

  • Strong understanding of monitoring visit documentation and site management processes.