176 Document Review jobs available for remote work from home. Apply for positions such as Real Estate Paralegal, Director, Regulatory Affairs Liaison, Vaccines & Infectious Diseases, Sr CRA II (Site Care Partner) - Sponsor Dedicated - Buenos Aires, 100% remote - Experience in oncology (ideally), and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Real Estate Paralegal supports the legal department by managing real estate development, financing, and corporate transactions. Responsibilities include coordinating due diligence, drafting closing documents, and serving as a liaison between internal teams and external partners.
The Director is responsible for developing and implementing global regulatory strategies for vaccines and infectious disease projects to ensure timely approvals. They lead cross-functional teams, manage interactions with regulatory agencies like the FDA, and provide expert guidance throughout the drug life cycle.
The Senior CRA II 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 patient recruitment and retention strategies.
Review contributor submissions across text and video formats against project-specific guidelines to ensure accuracy and quality. Identify and escalate suspicious or low-quality content while providing constructive feedback to contributors.
The Director of Medical Writing will produce high-quality, strategically aligned regulatory documents to support clinical development programs. They will manage document review processes, coordinate with cross-functional teams, and ensure compliance with global regulatory requirements.
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Review human pose keypoint annotations on thermal images to ensure accuracy, consistency, and anatomical plausibility. Provide actionable feedback to annotators and track performance trends to maintain high-quality data standards.
The Claims Contract Attorney will review and analyze claim forms, supporting documentation, and related materials for product liability, class action, and mass tort matters. They will also prepare professional responses to inquiries from claimants and counsel while ensuring compliance with project requirements.
The attorney will support ongoing document review cases using the Relativity platform under the supervision of a managing attorney. This role involves full-time work for a federal client, requiring adherence to standard business hours.
The Senior Clinical Research Associate conducts site monitoring visits in the Netherlands and Belgium to ensure protocol compliance and data integrity. They provide leadership and guidance to the clinical team while managing study budgets and site-related issues.
The Senior Clinical Research Associate conducts site monitoring visits, ensures protocol compliance, and provides leadership to the clinical team. They are responsible for managing study budgets, resolving site issues, and maintaining high standards of data integrity and regulatory adherence.
The Program Manager serves as the primary point of contact for the Contracting Officer's Representative and oversees all contractor work under the task order. They lead a distributed review organization responsible for evaluating cybersecurity plans and compliance for maritime facilities.
The Senior Director will lead merchant boarding, underwriting, and risk operations while modernizing workflows through automation and AI. They will also oversee portfolio monitoring, regulatory compliance, and the development of risk strategies for future embedded lending products.
Lead the merchant boarding, underwriting, and risk operations functions while modernizing workflows through automation and AI. Partner with cross-functional teams to define risk appetite and operationalize data for payments and future embedded lending products.
Review verification submissions for compliance, conduct KYC checks, and analyze digital footprints to prevent fraud. Perform quality assurance on verification decisions and collaborate with internal teams to streamline onboarding processes.
The project attorney will conduct complex document reviews, perform legal research, and analyze privileged or responsive documents. They are also responsible for maintaining accurate time records and drafting memoranda regarding project status.
The Project Monitor III manages federal financial assistance awards by monitoring recipient progress, deliverables, and milestones while performing technical evaluations. They also oversee award closeouts, prepare briefings for federal teams, and ensure compliance with DOE requirements.
The Project Monitor II will provide engineering, technical, and operational support for Department of Energy programs, including monitoring project scope, schedule, and budget. They will perform technical evaluations, review financial reports, and ensure compliance with federal award requirements.
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The Medical Science Liaison acts as a field-based scientific expert to support oncology therapeutic objectives and build relationships with healthcare professionals. They are responsible for executing territory plans, supporting clinical research initiatives, and providing disease state education.
The role involves developing and managing scientifically rigorous medical content, including scientific response documents and training materials for life sciences clients. The manager will lead content development processes, facilitate medical, legal, and regulatory reviews, and collaborate with cross-functional teams to ensure high-quality, compliant deliverables.
The Department Manager will provide technical leadership, manage structural engineering resources, and oversee project execution for heavy industrial and infrastructure projects. Responsibilities include hiring and developing staff, establishing quality control standards, and supporting business development initiatives.
The CRA II 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.
The Senior CRA I 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 provide guidance to site staff to ensure project objectives are met.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the clinical trial lifecycle.
The Senior Clinical Trial Manager provides end-to-end operational leadership for early-phase oncology studies from start-up through close-out. This role manages cross-functional teams, vendor performance, and study budgets while ensuring compliance with global regulatory requirements.
The Senior Process Improvement Professional manages operational processes and supports the execution of key regulatory and operational initiatives within the CPES team. This role ensures work is completed on schedule, maintains process documentation, and facilitates alignment across cross-functional stakeholders.
The consultant supports the Agricultural Advisory Service team by preparing financial and tax planning materials for high-net-worth clients. They are responsible for gathering client information, drafting reports, and coordinating meeting logistics to ensure a seamless advisory experience.
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Conduct first- and second-level privilege, relevance, and confidentiality reviews of electronic documents for class action litigation. Identify key evidence, apply issue coding protocols, and draft summaries for senior legal staff.
Document reviewers will analyze complex litigation documents using electronic platforms to code for relevancy, confidentiality, and privilege. They are also responsible for conducting quality control checks and assisting with the preparation of privilege and redaction logs.
Document reviewers will analyze complex litigation documents using electronic platforms to code for relevancy, confidentiality, and privilege. They are also responsible for conducting quality control checks and assisting with the preparation of privilege and redaction logs.
Document reviewers will analyze complex litigation documents using electronic platforms to code for relevancy, confidentiality, and privilege. They are also responsible for conducting quality control checks and assisting with the preparation of privilege and redaction logs.
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