Remote Document Review Jobs

124 Document Review jobs available for remote work from home. Apply for positions such as CRA I/II - Beijing, Principal Software Engineer - U.S. (remote) , Legal Assistant, General Counsel, 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
DISCO is hiring for remote Principal Software Engineer - U.S. (remote)

Principal Software Engineer - U.S. (remote)

DISCO · Full Time · 1 Week Ago
DISCO
🌎 United States ⭐ 10+ yrs exp πŸ’Ό Software Development Principal Software Engineer
The Principal Software Engineer drives the evolution of system architecture using Distributed Domain Driven Design to ensure scalability and robustness. They provide strategic leadership for quality attributes and offer project-embedded consultation to promote best practices and design patterns.
Earthjustice is hiring for remote Legal Assistant, General Counsel

Legal Assistant, General Counsel

Earthjustice · Full Time · 1 Week Ago
Earthjustice
🌎 United States πŸ’΅ $65000 - $84900 per year ⭐ 2-5 yrs exp πŸ’Ό Legal General Counsel
Provide legal, operational, and administrative support to the Office of General Counsel, focusing on litigation management and internal legal operations. Key duties include managing contract lifecycles, maintaining electronic record repositories, and providing executive administrative support to attorneys.
CACI International is hiring for remote Paralegal - Omaha, NE

Paralegal - Omaha, NE

CACI International · Full Time · 1 Week Ago
CACI International
🌎 United States ⭐ 2-5 yrs exp πŸ’Ό Legal Paralegal
Provide comprehensive litigation support and witness management for USAO attorneys, including coordinating travel and court appearances. Handle the preparation, filing, and archiving of legal documents and assist with trial preparation and in-court room support.
Syneos Health is hiring for remote CRA II - Sponsor Dedicated - Oncology / Neurology (Home-Based: Savannah, GA / Augusta, GA / Charleston, SC)
🌎 Germany ⭐ 2-5 yrs exp πŸ’Ό Others
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

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Syneos Health is hiring for remote CRA II - Sponsor Dedicated - Oncology / Neurology (Home-Based - Boston, MA)

CRA II - Sponsor Dedicated - Oncology / Neurology (Home-Based - Boston, MA)

Syneos Health · Full Time · 1 Week Ago
Syneos Health
🌎 United States ⭐ 2-5 yrs exp πŸ’Ό Others
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

Technical Writer

Kaiva Tech · Full Time · 1 Week Ago
Kaiva Tech
🌎 United States ⭐ 2-5 yrs exp πŸ’Ό Writing Technical Writer
Develop, revise, and maintain technical and regulatory documentation to support OIFSSP program initiatives, specifically the BRIDGE and TCS retail food programs. Collaborate with subject matter experts to translate complex regulatory information into clear, concise, and audience-appropriate materials.
Precision Medicine Group is hiring for remote Regulatory and Site Start Up Specialist

Regulatory and Site Start Up Specialist

Precision Medicine Group · Full Time · 1 Week Ago
Precision Medicine Group
🌎 Taiwan ⭐ 2-5 yrs exp πŸ’Ό Legal
Responsible for the timely delivery of site activation readiness and the preparation of submission dossiers for Competent Authorities and Ethics Committees. The role involves coordinating with CRAs and project teams to manage essential documents and ensure compliance with local and international regulations.

Regulatory and Site Start Up Specialist

Precision for Medicine · Full Time · 1 Week Ago
Precision for Medicine
🌎 Taiwan ⭐ 2-5 yrs exp πŸ’Ό Legal
Responsible for the timely delivery of site activation readiness and the preparation of submission dossiers for Competent Authorities and Ethics Committees. Coordinates with CRAs and project teams to manage essential documents and ensure compliance with local and international regulations.

Regulatory and Site Start Up Specialist

Precision for Medicine · Full Time · 2 Weeks Ago
Precision for Medicine
🌎 China ⭐ 2-5 yrs exp πŸ’Ό Legal
Responsible for managing regulatory submissions to Competent Authorities and Ethics Committees to ensure timely site activation. The role involves coordinating essential document collection, reviewing informed consent forms, and supporting budget and contract negotiations.
Precision Medicine Group is hiring for remote Regulatory and Site Start Up Specialist

Regulatory and Site Start Up Specialist

Precision Medicine Group · Full Time · 2 Weeks Ago
Precision Medicine Group
🌎 China ⭐ 2-5 yrs exp πŸ’Ό Legal
Manage regulatory and site start-up activities, including submissions to Competent Authorities and Ethics Committees to ensure timely site activation. Coordinate the collection of essential documents and support budget and contract negotiations for clinical trials.

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New remote document review jobs delivered to your inbox

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Cognitive Research Corporation is hiring for remote Senior Clinical Research Associate - CNS

Senior Clinical Research Associate - CNS

Cognitive Research Corporation · Full Time · 2 Weeks Ago
Cognitive Research Corporation
🌎 United States ⭐ 5-10 yrs exp πŸ’Ό Healthcare
Oversees the execution of clinical trials at investigative sites, acting as a liaison between the sponsor and sites to ensure data integrity and participant safety. Responsibilities include site initiation, monitoring, close-out, and mentoring junior staff.
Syneos Health is hiring for remote Clinical Research Associate - Sponsor Dedicated - Bilingual

Clinical Research Associate - Sponsor Dedicated - Bilingual

Syneos Health · Full Time · 2 Weeks Ago
Syneos Health
🌎 Canada ⭐ 5-10 yrs exp πŸ’Ό Healthcare
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File and Trial Master File.
Alira Health is hiring for remote Lead Clinical Research Associate

Lead Clinical Research Associate

Alira Health · Full Time · 2 Weeks Ago
Alira Health
🌎 United States πŸ’΅ $110K - $130K per year ⭐ 5-10 yrs exp πŸ’Ό Healthcare
The Lead CRA provides oversight, leadership, and guidance in the management and execution of clinical trial monitoring to ensure quality and compliance. Responsibilities include mentoring field CRAs, conducting site visits, and collaborating with cross-functional teams to resolve monitoring issues.

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