260 Document Review jobs available for remote work from home. Apply for positions such as Paralegal (Primarily Remote) - Major Public Inquiry, Senior Clinical Research Associate (Oncology) - UK (Remote) - FSP, Technical Writer, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The paralegal will conduct document review and disclosure exercises using e-disclosure platforms for a major public inquiry. They will also assist in the preparation of witness statements and manage sensitive material across various archive locations.
The Senior Clinical Research Associate will oversee monitoring activities at investigator sites to ensure clinical trial quality, data integrity, and regulatory compliance. They will collaborate with site personnel and project teams to support study execution and maintain inspection readiness.
The Technical Writer will develop and maintain complex acquisition and policy documentation, including RFPs, PWSs, and SOPs, to support federal healthcare programs. They will facilitate working sessions with stakeholders to translate operational requirements into clear, actionable, and compliant government documentation.
The attorney will perform document review, privilege review, and legal research for various projects. They will also assist with foreign language translation and utilize electronic document review technology.
Independently manage concurrent eDiscovery and litigation projects within the Relativity platform from processing through production. Provide consultative support to clients by developing custom workflows and ensuring high-quality work products throughout the litigation lifecycle.
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The Senior eDiscovery Project Manager will independently manage complex litigation projects within the Relativity platform, overseeing the full EDRM lifecycle from processing to production. They will also provide expert consultation to clients, develop custom workflows, and support junior team members through training and technical escalation.
Independently manage concurrent eDiscovery and litigation projects within the Relativity platform from processing through production. Provide consultative support to clients by developing custom workflows and ensuring high-quality work products throughout the litigation lifecycle.
The Associate Project Manager will administer and manage casework throughout the EDRM, focusing on the Relativity platform. They will collaborate with internal and external teams to execute complex litigation projects from data processing through production.
The Associate Project Manager will administer and manage casework throughout the EDRM, focusing on the Relativity platform. They will work closely with internal and external teams to handle document review, production, and data searching workflows in a deadline-driven environment.
Conduct and oversee clinical trial site monitoring, including site visits, source data verification, regulatory documentation, investigational product accountability, and compliance with protocols, ICH GCP, and applicable regulations. Guide and mentor CRA colleagues, coordinate with sponsors and cross-functional teams, resolve site and data issues, and support study planning, reporting, and quality.
Independently conduct and oversee clinical trial site monitoring, including site visits, source document verification, regulatory documentation, investigational product accountability, and compliance with protocols, ICH GCP, and applicable regulations. Guide and mentor CRA team members, coordinate with sponsors and cross-functional teams, resolve site and data issues, and support study planning, recruitment, reporting, and quality activities.
Conduct and oversee clinical trial site monitoring activities in Belgium and the Netherlands, including site visits, source document verification, regulatory documentation, investigational product accountability, and compliance with protocols and GCP requirements. Provide guidance and mentoring to CRA colleagues, coordinate with sponsors and cross-functional teams, resolve site issues, and support study quality, recruitment, and delivery.
Independently conduct and oversee clinical trial site monitoring, including site visits, source data verification, regulatory documentation, investigational product accountability, and compliance with protocols, ICH GCP, and applicable regulations. Guide and mentor CRA team members, coordinate with sponsors and cross-functional teams, resolve site and study issues, and support study planning, reporting, recruitment, and quality.
Own the delivery position behind tenant pursuits across powered land, powered shell, and turnkey data center offerings, validating capacity, schedules, costs, risks, and proposed agreement terms against delivery plans. Coordinate diligence and negotiations, maintain campus capacity and pipeline views, and transfer executed commitments and assumptions to the delivery organization.
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Review documents in Relativity following an established protocol and identify and capture personally identifiable information (PII) and protected health information (PHI). Work with the Review Manager and team to address questions and meet review requirements.
Oversee clinical-trial safety surveillance, serious adverse event case processing, signal assessment, aggregate safety reporting, and compliance with global pharmacovigilance requirements. Manage PV vendors and CROs, support safety committees and health authority interactions, maintain safety documentation and quality processes, and guide the growing pharmacovigilance function.
Provide first-line technical support to customers by diagnosing software, hardware, installation, and configuration issues, answering product and postal requirements questions, and documenting resolutions. Own customer issues through resolution, escalating complex cases and collaborating with internal teams while maintaining support resources and identifying product improvements.
The Senior Clinical Research Associate oversees the execution of clinical trials at investigative sites, acting as a liaison between the sponsor and site staff. They are responsible for monitoring sites, ensuring data integrity, managing study documentation, and mentoring junior staff.
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The Loan Processor is responsible for reviewing and inputting financial documentation to assess business creditworthiness using internal systems. They also conduct final due diligence and ensure all funding conditions are met to facilitate accurate and timely deal funding.
The manager oversees the operational infrastructure for the Real Estate Legal Department, focusing on workflow automation, contract administration, and AI-enabled process design. They collaborate with cross-functional teams to streamline legal processes and ensure accurate documentation across a large property portfolio.
The Sr. Facility Condition Advisor conducts visual assessments of building systems to determine current condition, remaining useful life, and repair costs in accordance with ASTM E2018-24 standards. They are responsible for gathering data, documenting physical deficiencies, and preparing comprehensive facility condition reports to support long-term capital planning.
The Sr. Facility Condition Advisor conducts visual assessments of building systems to determine current condition, remaining useful life, and repair costs in accordance with ASTM E2018-24 standards. They are responsible for documenting physical deficiencies and preparing comprehensive facility condition reports to support long-term capital planning.
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