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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Frank Scottile Blvd |LA :
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Bangor | Brewer |Maryland :
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Andover | Billerica | Boston | Cambridge | Devens | Lexington | Massachusetts | Medford and Somerville | Rockland |Michigan :
Detroit | Houghton Lake | Macomb | Southfield |Minnesota :
Duluth | Eden Prairie | Fridley | Hibbing | Maple Grove | Minneapolis and St. Paul, Minnesota. | Minnetonka | St.Paul |Missouri :
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Bayreuth | Erlangen | Munich | Regensburg | Wurzburg |Berlin :
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Berlin |Germany :
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Frankfurt | Harveysburg |Lower Saxony :
Gottingen | Hannover | Leipzig |Mecklenburg Vorpommern :
Rostock |Munich :
Bavaria |North Rhine Westphalia :
Aachen | Bielefeld | Bochum | Bonn | Cologne | Dortmund | Duisburg | Dusseldorf | Munster |Rhineland Palatinate :
Ingelheim am Rhein | Mainz |Rotherbaum :
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Wavre |BULGARIA :
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Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Galway |Meath :
Dunboyne |Republic of Ireland :
Cork | Dublin | Limerick | Waterford |Tipperary :
Ballydine |Ulster :
Donegal |China :
China | Quarry Bay |Hubei :
Wuhan |Liaoning :
Dalian |Republic of China :
Beijing |Shanghai Sai :
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Osaka | Tokyo |Zhejiang :
Hangzhou |Melbourne :
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Ballina | Sydney |Queensland :
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Arkansas | Remote Australia |Republic of Western Australia :
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Amsterdam |Netherlands :
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Haarlem |North Brabant :
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Leiden |North Yorkshire :
Harrogate |Oxfordshire :
Witney |South Yorkshire :
Sheffield |United Kingdom :
England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |Buenos Aires :
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Vienna |Antwerp :
Heist op den Berg |Brussels :
Brussels |Flemish Brabant :
Zaventem |Bosnia and Herzegovina :
Sarajevo |Sofia City :
Sofia |Canada :
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Richmond Hill | Australia | Uxbridge | North York | Mississauga | Renfrew |Quebec :
Montreal |Chile :
Santiago |Republic of Colombia :
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Croatia |Zagreb :
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Italy |Lombardy :
Rho |Japan :
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Almaty |Remote Korea :
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