2,591 Clinical Research jobs available for remote work from home. Apply for positions such as FSP - Project Manager II / Sr. Project Manager - Oncology & Ophthalmology, Manager, FSA, Regulatory Technician, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Senior Project Manager oversees domestic and global clinical projects, ensuring delivery within scope, schedule, and budget while managing risks and quality. They also serve as the primary client contact, lead cross-functional teams, and may provide line management and talent development for staff.
Lead teams in delivering high-quality feasibility assessments and efficient site activation for global clinical trials. Oversee project strategies, monitor performance metrics, and provide coaching to staff to ensure operational excellence.
The Regulatory Technician manages data and document uploads within the Clinical Trials Information System (CTIS) while ensuring regulatory compliance. They also coordinate submission tasks, perform quality control reviews, and maintain communication with internal and external stakeholders.
Conduct PK/PD data analysis using non-compartmental analysis and support modeling and simulation tasks. Contribute to clinical trial protocol development, statistical analysis plans, and the authoring of regulatory documents and study reports.
The IT Operations Lead manages the daily delivery of virtual desktop and end-user computing support for global healthcare revenue cycle operations. This role involves leading a distributed team, overseeing service-level performance, and acting as a major-incident commander for technical outages.
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You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Additionally, you will conduct site visits, resolve performance issues, and collaborate with cross-functional teams to ensure accurate data collection.
The associate will assist in the preparation of client proposals, including cost estimates, timelines, and scope of work documents. They will also collaborate with cross-functional teams to gather information and conduct research to inform proposal development.
You will conduct clinical trial monitoring activities including site visits, protocol compliance, and data integrity maintenance. Additionally, you will collaborate with investigators and site staff to ensure smooth study conduct and high-quality data reporting.
The Licensing Manager leads the end-to-end execution of COA and eCOA licensing services for global clinical studies while acting as a subject matter expert for clients. They are responsible for managing delivery teams, ensuring operational excellence, and supporting commercial growth through proposal development and client expansion.
The Associate Director provides strategic and operational leadership for the Study Start-Up function, overseeing activities from study award through site activation. This role manages the team, ensures cross-functional alignment, and maintains compliance with regulatory standards and sponsor expectations.
The Associate Director provides strategic and operational leadership for the Clinical Trial Management team, overseeing trial execution and ensuring compliance with protocols and regulations. They are responsible for mentoring staff, managing study budgets and timelines, and fostering cross-functional collaboration to drive operational excellence.
The Oncology Provider Account Manager will build and maintain relationships with oncology providers to educate them on AI-powered clinical trial matching services. The role involves conducting field visits to clinics to drive physician awareness, referral processes, and engagement outcomes.
The Clinical Research Associate performs on-site and remote monitoring activities to ensure site compliance and data quality throughout clinical trials. They are responsible for training site staff and supporting regulatory or ethics committee submissions.
The Senior Safety Technology Analyst will lead the configuration, implementation, and operational support of pharmacovigilance safety systems. They will also manage system integrations, ensure regulatory compliance, and collaborate with cross-functional teams to drive safety technology excellence.
The Safety Technology Analyst will manage and configure safety databases while ensuring regulatory compliance and operational excellence. They will collaborate with cross-functional teams to resolve technical issues and support system handovers throughout the clinical trial lifecycle.
The Site Contracts Lead oversees the end-to-end preparation, negotiation, and execution of clinical trial agreements and budgets. They also provide guidance to contract negotiators and collaborate with legal and finance teams to ensure alignment on contract language and risk.
The specialist will process and submit safety reports to regulatory authorities while ensuring compliance with SOPs and project requirements. They will also liaise with functional team members and healthcare professionals to address project-related issues and provide feedback on operational performance.
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The Project Coordinator supports study execution from startup through closeout by managing documentation, database updates, and project tracking. They also facilitate communication between cross-functional teams and sponsors while ensuring project milestones and quality standards are met.
The Clinical Trial Coordinator manages site readiness, regulatory compliance, and the maintenance of essential study documents across a multi-country cluster. They act as the central connector for clinical teams while overseeing logistics, trial systems, and document excellence to ensure inspection readiness.
The Senior Site Contracts Specialist independently leads the negotiation, execution, and management of clinical trial agreements and study budgets. This role acts as a key liaison between investigative sites, sponsors, and study teams to ensure timely study startup and effective issue resolution.
You will develop global regulatory strategies for clinical trial applications and marketing authorizations while providing guidance to cross-functional teams. Additionally, you will manage regulatory submissions, ensure compliance with global standards, and participate in regulatory intelligence activities.
The Informed Consent Specialist II is responsible for preparing, reviewing, and approving Subject Information Sheets and Informed Consent Forms in accordance with regulatory guidelines and ICON SOPs. They also serve as a subject matter expert, mentor new hires, and coordinate with sponsors and ethics committees to ensure study start-up and maintenance activities are completed accurately.
You will lead clinical trial initiation activities, including the preparation and submission of regulatory documents to ethics committees and agencies. Additionally, you will coordinate with internal and external stakeholders to ensure study compliance and provide guidance on regulatory best practices.
You will lead clinical trial initiation activities, including the preparation and submission of regulatory documents to ethics committees and agencies. Additionally, you will coordinate with internal and external stakeholders to ensure compliance and streamline site start-up processes.
The Territory Account Manager is responsible for developing strategic relationships with key opinion leaders and distribution partners to drive sales within a geographic territory. They will manage the full sales process for CRO projects and maintain accurate records in the CRM system to monitor funnel growth.
The Senior Study Leader co-leads cross-functional clinical trial teams to deliver global clinical studies according to the Operational Execution Plan and protocol. They are responsible for proactive operational planning, risk management, budget oversight, and fostering an agile, collaborative team environment.
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The Patient Navigator will support clinical trial participants through inbound and outbound communication, providing emotional support and managing study logistics. They will also conduct digital campaign prescreening to determine participant eligibility and maintain accurate documentation in helpdesk systems.
The Patient Navigator will support clinical trial participants through inbound and outbound communication, providing emotional support and managing study logistics. They will also conduct digital campaign prescreening to determine participant eligibility and maintain accurate documentation in helpdesk systems.
The Director of Business Development is responsible for driving sales strategies, identifying new business opportunities, and managing client relationships within the Internal Medicine and Neuroscience sector. They will coordinate proposal processes, lead bid defense meetings, and monitor competitor activities to ensure company growth.
The Senior Site Specialist serves as a key operational point of contact for investigator sites, managing essential document collection and site-level activities. They also provide mentorship to junior team members and contribute to process improvement initiatives to streamline site workflows.
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