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Document Quality Reviewer Ii

0-4 years
Not Disclosed
10 Nov. 18, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Document Quality Reviewer II – Remote, India

Location: India (Remote)
Job Type: Full-Time, Regular
Experience Required: 0–4+ years (Fresher to Experienced)


About Parexel

Parexel is a global leader in clinical research and medical writing, dedicated to advancing healthcare by providing high-quality, compliant scientific documentation. As part of Parexel’s Medical Writing team, the Document Quality Reviewer II ensures the accuracy, consistency, and clarity of clinical research documents while supporting regulatory compliance and scientific excellence.

We foster a culture of collaboration, inclusivity, and continuous learning, offering mentorship, job shadowing, rotations, and growth opportunities aligned with global standards.


Role Overview

The Document Quality Reviewer II (DQR II) is responsible for reviewing and editing clinical documents, ensuring the highest quality standards in grammar, syntax, scientific content, and formatting. This role requires attention to detail, knowledge of clinical research concepts, and proficiency in applying style guides and regulatory requirements. The DQR II works independently on complex documentation, including clinical study reports, protocols, patient narratives, informed consent forms, regulatory responses, and investigator brochures.


Key Responsibilities

Quality Control & Review

  • Perform thorough quality reviews of clinical documents to ensure accuracy, clarity, logical flow, and adherence to style guides or client-specific conventions.

  • Edit for language, grammar, technical terminology, data accuracy, and scientific content.

  • Ensure consistency and integrity across document sections and between related documents.

  • Conduct independent quality review of complex clinical documentation, identifying errors, inconsistencies, or formatting issues.

  • Document review findings and escalate significant issues to authors or team leads.

  • Participate in resolving document discrepancies and implementing corrective actions.

Process & Compliance

  • Attend mandatory training, project-specific, and corporate learning sessions.

  • Stay updated on professional trends, regulatory requirements, and clinical research best practices.

  • Provide guidance and mentorship to less experienced team members or new hires.

  • Evaluate and recommend improvements to document review processes to reduce recurring errors.

Collaboration & Communication

  • Work closely with medical writers, project teams, and stakeholders to ensure timely delivery of high-quality documents.

  • Participate in departmental meetings, knowledge-sharing initiatives, and process improvement projects.

  • Apply a client-focused approach while maintaining proactive, solutions-driven communication.


Required Skills & Competencies

  • Exceptional written and verbal communication skills with a strong command of English.

  • Rigorous attention to detail and excellent proofreading and copyediting capabilities.

  • Ability to manage multiple tasks, prioritize effectively, and deliver consistently high-quality output.

  • Familiarity with clinical research concepts, regulatory documents, and ICH-GCP guidelines.

  • Client-oriented, collaborative, and adaptable to dynamic project requirements.

  • High numeracy skills and ability to interpret statistical or clinical data is an advantage.

  • Proficiency in Microsoft Office and willingness to learn document management systems and collaborative authoring tools.


Education & Experience

  • Bachelor’s degree in Life Sciences, Health Sciences, or related field (required).

  • Experience: Fresher to 4+ years in medical writing, pharmaceutical, or clinical research environments.

  • Prior experience in proofreading, quality review, or regulatory documentation is an advantage.


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