8,072 Agile jobs available for remote work from home. Apply for positions such as Marketing & Operations Strategy Co-Op, Application Software Engineer, Senior, Medical/Clinical Scientist - Immunology -Dermatology (Sponsor-dedicated/Remote), and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The co-op will conduct financial and operational analysis to support strategic initiatives and business growth. They will collaborate with cross-functional teams to identify performance trends and implement business transformation strategies.
The Senior Application Software Engineer will design, develop, test, and implement new or existing application software while leading Agile methodologies. They will also ensure rigorous application of cybersecurity policies and integrate hardware and software components to support the FLITES system.
The Medical/Clinical Scientist develops medical plans and performs regular medical data reviews to identify risks and trends. They serve as the primary interface between internal teams, customers, and vendors to ensure project milestones and data integrity are met.
The Clinical/Medical Scientist will develop medical plans and perform regular medical data reviews to identify risks and trends in clinical study data. They will serve as a primary interface between internal teams and customers to ensure project milestones and data integrity are maintained.
Provide white-glove technical support to clinical trial sites regarding credentialing, authentication, and platform access. Facilitate virtual training sessions and troubleshoot system access issues to ensure seamless clinical trial operations.
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The Senior Clinical Research Associate 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 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 ensure patient safety and data integrity throughout the study.
The Clinical Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol compliance and data integrity throughout the study lifecycle. They coordinate with cross-functional teams to meet study milestones, manage risks, and oversee the performance of clinical research associates and central monitors.
The Site Contracts Specialist II manages the end-to-end contract process, including negotiating budgets and agreements for clinical trials. They also provide functional guidance to team members, ensure compliance with SOPs, and collaborate with internal and external stakeholders to facilitate contract execution.
The Site Payment Specialist manages project files, study information, and financial reporting, including investigator payments and site invoices. They also facilitate internal and external meetings, track key performance indicators, and provide support for audits and quality assurance activities.
The Clinical Project Manager II supports late-phase Hematology and Immunology portfolios by managing operational tasks and liaising with CROs and vendors. They are responsible for developing clinical trial documents, maintaining project team communication, and ensuring study timelines are met.
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 patient recruitment and retention strategies.
The Project Manager II supports the clinical trial operational team by managing CROs and ancillary vendors to ensure study alignment. They are responsible for developing clinical trial documents, including study manuals and Master ICF templates, while overseeing study timelines.
The Medical Scientist will collaborate with cross-functional teams to provide deep expertise and drug development insights to support customer goals. They are responsible for navigating complex drug development processes and delivering innovative solutions within a competitive environment.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure compliance with regulatory standards and study protocols. They manage site-level activities, verify clinical data accuracy, and act as a primary liaison between the study site and the project team.
The Senior Clinical Project Manager will oversee the development of clinical trial documentation, including protocols and regulatory reports, while managing trial timelines and budgets. They are responsible for site selection, vendor coordination, and implementing risk mitigation and recruitment plans.
The Site Contracts Lead manages the end-to-end contract process, including drafting, negotiating, and executing clinical trial agreements and budgets. They also provide functional guidance to team members, ensure compliance with SOPs, and act as a liaison between internal departments and external sites.
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The Regulatory Labeling Manager will support labeling negotiations with health authorities and interpret safety data to inform labeling updates. They are responsible for preparing labeling components for eCTD submissions and utilizing structured content authoring tools.
The Senior Project Manager will lead cross-functional teams using agile methodologies to deliver technical projects on time and within budget. Responsibilities include managing project plans, facilitating scrum ceremonies, and proactively removing impediments to ensure continuous workflow.
The Project Manager will lead cross-functional teams using agile methodologies to deliver technical projects on time and within budget. They are responsible for facilitating agile ceremonies, managing project health, and removing impediments to ensure continuous workflow.
Collaborate with public sector clients to design and implement modernized HCM and payroll systems. Facilitate stakeholder meetings, analyze business operations, and support project delivery through Agile methodologies.
The Software Engineer is responsible for designing, developing, and maintaining software applications throughout the entire development lifecycle. They will collaborate with cross-functional teams to refine requirements and lead coding efforts for specific modules.
The Lead Software Engineer will design, develop, and implement complex full-stack software features while mentoring junior team members. They are responsible for maintaining high-quality code standards, collaborating with cross-functional teams, and resolving complex technical issues.
The Quality Engineer will design, develop, and maintain test plans and automation frameworks for the Warehouse Edge platform. They will collaborate with cross-functional teams to ensure software quality and reliability across complex warehouse workflows.
The Regulatory Consultant will manage and track regulatory submissions while maintaining content plans within Veeva Vault RIM. They will also coordinate submission activities and translate project timelines into actionable plans using Smartsheet and Microsoft Project.
The Senior Manager will lead cross-functional regulatory project management activities for global submissions, ensuring compliance with FDA, EMA, and ICH guidelines. They are responsible for managing multiple marketing applications and lifecycle management submissions from initial filing through to final approval.
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The Clinical Operations Specialist assists clinical monitoring staff with site management activities and ensures compliance with study protocols and regulatory guidelines. They are also responsible for maintaining the Trial Master File, tracking clinical documentation, and coordinating site supplies.
The Sr Project Specialist manages study documentation, including TMF, regulatory files, and financial reports, while ensuring compliance with clinical research standards. They also facilitate internal and external meetings, track KPIs, and provide support for audits and quality assurance activities.
The Regulatory Strategist will lead and coordinate regulatory submissions and life-cycle management procedures for Latin American markets. They will act as a local regulatory expert, providing guidance to cross-functional teams and ensuring compliance with regional health authority requirements.
The Cardiovascular Disease Specialist will drive patient impact by serving as the primary contact for healthcare customers and executing territory-level business plans. They will collaborate with internal teams to deliver patient-focused solutions while maintaining product knowledge and compliance standards.
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