Remote Document Review Jobs

124 Document Review jobs available for remote work from home. Apply for positions such as Senior CRA in Oncology Phase I - Sponsor dedicated - Home Based in Paris Area, Sr CRA for FSP BU based in South Korea, Commercial Compliance Senior Specialist, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.

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Remote Document Review Jobs (124)

Tags = document-review
Syneos Health is hiring for remote Senior CRA in Oncology Phase I - Sponsor dedicated - Home Based in Paris Area

Senior CRA in Oncology Phase I - Sponsor dedicated - Home Based in Paris Area

Syneos Health · Full Time · 3 hours ago
Syneos Health
🌎 France ⭐ 5-10 yrs exp 💼 Others
The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
Syneos Health is hiring for remote Sr CRA for FSP BU based in South Korea

Sr CRA for FSP BU based in South Korea

Syneos Health · Full Time · 10 hours ago
Syneos Health
🌎 South Korea ⭐ 5-10 yrs exp 💼 Others
The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
Viatris is hiring for remote Commercial Compliance Senior Specialist

Commercial Compliance Senior Specialist

Viatris · Full Time · Yesterday
Viatris
🌎 United States 💵 $55000 - $105K per year ⭐ 2-5 yrs exp 💼 Legal
The role involves developing and executing compliance training programs, drafting company policies, and conducting field ride-alongs to monitor adherence to regulatory standards. The specialist will also serve as a primary compliance partner for the U.S. Brand field force, providing guidance and performing quarterly monitoring and auditing activities.

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Syneos Health is hiring for remote CRA II or Sr CRA assigned to client (FSP) - Bogotá, Barranquilla, Medellín - Colombia Home-Based
🌎 Colombia ⭐ 2-5 yrs exp 💼 Others
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the study lifecycle.
KLDiscovery is hiring for remote Sr. Litigation Data Analyst

Sr. Litigation Data Analyst

KLDiscovery · Full Time · 3 Days Ago
KLDiscovery
🌎 United States ⭐ 2-5 yrs exp 💼 Software Development Data Analyst
The Senior Litigation Data Analyst provides advanced technical support and troubleshooting for Relativity platforms while designing complex workspace structures and workflows. They also mentor junior team members, ensure quality deliverables, and act as a point of escalation for complex client requests.
Parexel is hiring for remote Documentation Specialist (Medical/Technical Writing) - South Africa - FSP
🌎 South Africa ⭐ 2-5 yrs exp 💼 Writing
The Documentation Specialist supports the preparation and coordination of clinical development documents, including clinical trial reports, protocols, and investigator brochures. They also manage document workflows within the Electronic Document Management System and coordinate project timelines with cross-functional teams.
Parexel is hiring for remote Documentation Specialist (Medical/Technical Writing) - UK or Ireland - FSP
🌎 Ireland, United Kingdom ⭐ 2-5 yrs exp 💼 Writing
The Documentation Specialist will support the preparation and coordination of clinical development documents, including protocols, reports, and submission materials. They will also manage document workflows within the EDMS, coordinate timelines, and ensure high-quality documentation through rigorous quality control.
Parexel is hiring for remote Documentation Specialist (Medical/Technical Writing) - France - FSP
🌎 France ⭐ 0-2 yrs exp 💼 Writing
The Documentation Specialist will support the preparation and coordination of clinical development documents, including protocols, reports, and investigator brochures. They will also manage document workflows, track project deliverables, and assist with quality control and administrative processes within the EDMS.
Parexel is hiring for remote Medical Writer - Sponsor Dedicated - Remote

Medical Writer - Sponsor Dedicated - Remote

Parexel · Full Time · 3 Days Ago
Parexel
🌎 Italy ⭐ 2-5 yrs exp 💼 Writing Medical Writer
The Medical Writer will support the preparation and coordination of clinical development documents such as protocols, reports, and investigator brochures. They will also manage document workflows, coordinate timelines, and ensure high-quality documentation in compliance with sponsor procedures.

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Syneos Health is hiring for remote Tijdelijke CRA positie in Nederland

Tijdelijke CRA positie in Nederland

Syneos Health · Full Time · 3 Days Ago
Syneos Health
🌎 Netherlands ⭐ 2-5 yrs exp 💼 Others
The Clinical Research Associate (CRA) will perform site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They are responsible for managing site activities, verifying clinical data accuracy, and maintaining essential study documentation.
Parexel is hiring for remote Medical Writer - South Africa - FSP

Medical Writer - South Africa - FSP

Parexel · Full Time · 3 Days Ago
Parexel
🌎 South Africa ⭐ 2-5 yrs exp 💼 Writing Medical Writer
The Medical Writer will support the preparation and coordination of clinical development documents, including protocols, reports, and submission materials. They will also manage document workflows, coordinate timelines, and ensure quality control within the electronic document management system.
Parexel is hiring for remote Documentation Specialist / Medical Writer  - FSP

Documentation Specialist / Medical Writer - FSP

Parexel · Full Time · 3 Days Ago
Parexel
🌎 United Kingdom ⭐ 2-5 yrs exp 💼 Writing Medical Writer
The Documentation Specialist will develop and manage high-quality clinical and regulatory documents, including protocols and trial reports, throughout their lifecycle. They will also coordinate cross-functional review cycles, ensure compliance with standards, and manage document timelines within electronic systems.
Parexel is hiring for remote Medical Writer - UK or Ireland -  FSP

Medical Writer - UK or Ireland - FSP

Parexel · Full Time · 3 Days Ago
Parexel
🌎 Ireland, United Kingdom ⭐ 2-5 yrs exp 💼 Writing Medical Writer
The Medical Writer will support the preparation and coordination of clinical development documents such as protocols, reports, and investigator brochures. They will also assist with document workflow, quality control, and administrative tasks within the sponsor's electronic document management system.
Parexel is hiring for remote Medical Writer - France - FSP

Medical Writer - France - FSP

Parexel · Full Time · 3 Days Ago
Parexel
🌎 France ⭐ 2-5 yrs exp 💼 Writing Medical Writer
The Medical Writer will support the preparation and coordination of clinical development documents, including protocols, reports, and submission materials. They will also manage document workflows, coordinate review activities, and ensure compliance with sponsor procedures and regulatory standards.
Parexel is hiring for remote Senior Medical Writer - FSP

Senior Medical Writer - FSP

Parexel · Full Time · 3 Days Ago
Parexel
🌎 United Kingdom ⭐ 5-10 yrs exp 💼 Writing Medical Writer
The Senior Medical Writer is responsible for developing and managing high-quality clinical and regulatory documents, including protocols and clinical trial reports. They will coordinate review cycles, ensure compliance with project timelines, and facilitate alignment across cross-functional teams.
NAMSA is hiring for remote Field Senior Clinical Research Associate

Field Senior Clinical Research Associate

NAMSA · Full Time · 3 Days Ago
NAMSA
🌎 United States 💵 $68800 - $133K per year ⭐ 5-10 yrs exp 💼 Healthcare
The Field Senior Clinical Research Associate manages clinical site monitoring activities to ensure compliance with Good Clinical Practice and regulatory guidelines. They serve as the primary point of contact for investigative sites, supporting study start-up, enrollment, and data management tasks.
Parexel is hiring for remote Medical Writer II - FSP

Medical Writer II - FSP

Parexel · Full Time · 3 Days Ago
Parexel
🌎 United Kingdom ⭐ 2-5 yrs exp 💼 Writing Medical Writer
The Medical Writer II is responsible for developing and managing high-quality clinical and regulatory documents, including protocols and clinical trial reports. They will coordinate review cycles, ensure compliance with project timelines, and facilitate cross-functional team alignment throughout the document lifecycle.

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Conifer Realty LLC is hiring for remote Real Estate Paralegal

Real Estate Paralegal

Conifer Realty LLC · Full Time · 4 Days Ago
Conifer Realty LLC
🌎 United States 💵 $90000 - $100K per year ⭐ 5-10 yrs exp 💼 Legal Paralegal
The Real Estate Paralegal will manage real estate due diligence, acquisitions, and financing transactions while coordinating with internal and external stakeholders. They will also support construction contract administration, corporate entity maintenance, and provide general legal research and documentation support.
SINGLETON SCHREIBER LLP is hiring for remote Senior Litigation Paralegal

Senior Litigation Paralegal

SINGLETON SCHREIBER LLP · Full Time · 4 Days Ago
SINGLETON SCHREIBER LLP
🌎 United States 💵 $40 - $48 per hour ⭐ 5-10 yrs exp 💼 Legal Paralegal
The Senior Litigation Paralegal will manage litigation files, track deadlines, and coordinate discovery and deposition processes within the wildfire litigation team. They will also assist attorneys with document preparation, court filings, legal research, and trial support to ensure efficient case progression.

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