2,267 Clinical Research jobs available for remote work from home. Apply for positions such as Field CRA III (Field Clinical Research Associate III ), Site Manager, Clinical Trial Operations, Telehealth BCBA: Must live in Georgia, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Field Clinical Research Associate III manages clinical study sites to ensure protocol compliance, high-quality data collection, and audit readiness. They also collaborate on study documentation, provide mentorship to junior staff, and act as a liaison between the company and investigational sites.
Provide operational leadership and on-site support for multiple clinical research sites across the assigned region. Monitor study performance metrics, ensure regulatory compliance, and build strong relationships with investigators and site staff.
The BCBA will oversee and ensure the fidelity of ABA programs while providing coaching and mentorship to clinical leaders and behavior specialists. They are also responsible for managing treatment plans, ensuring compliance with clinical standards, and leading clinical development initiatives.
Perform manual, independent reviews of clinical trial interviews and scale administrations to ensure scoring accuracy and protocol adherence. Senior roles will also oversee site performance, interpret rater patterns, and manage targeted site interventions.
The Global Site Start-up Lead is responsible for the global execution and strategy of clinical trial site activation, ensuring compliance with SOPs and regulatory standards. They act as a subject matter expert, overseeing CRO performance and managing cross-functional team interactions to resolve site-related challenges.
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The specialist will lead clinical and selling activities for acute care monitoring technologies by partnering with sales teams to drive product evaluations and conversions. They are responsible for providing expert clinical education, supporting post-sale implementation, and developing reference accounts within their assigned territory.
The Clinical Market Development Specialist serves as a clinical expert to drive product adoption and sales within ICU, OR, and NICU/PICU environments. Responsibilities include leading clinical demonstrations, managing pre- and post-sale activities, and developing advocacy among key opinion leaders.
The Senior Clinical Data Manager will oversee all clinical data management activities from study start-up through database lock and closeout. They are responsible for managing relationships with CROs and vendors while ensuring data quality and regulatory compliance across the clinical portfolio.
The Medical Director provides strategic scientific leadership across client accounts and leads, mentors, and develops a team of scientific professionals. They are responsible for ensuring operational excellence, driving business growth, and maintaining the scientific integrity of high-impact client deliverables.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and the project team.
The Clinical Research Associate will monitor investigator sites to ensure protocol compliance, data accuracy, and regulatory adherence through risk-based monitoring. They will also manage site documentation, facilitate communication between stakeholders, and participate in investigator meetings and trial close-out activities.
The Field Senior Clinical Research Associate manages clinical site monitoring activities to ensure compliance with Good Clinical Practice and regulatory guidelines. They serve as the primary point of contact for investigative sites, supporting study start-up, enrollment, and data management tasks.
The Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure protocol compliance and data reliability. They will conduct risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and the project team.
The Clinical Research Associate II will conduct site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and data integrity. They will also collaborate with investigators and site staff while performing data review to maintain high-quality clinical study documentation.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They are responsible for ensuring regulatory compliance, managing safety reporting, and conducting study initiation visits.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure regulatory compliance and data integrity while overseeing site performance throughout the study lifecycle.
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The Principal Biostatistician will design and analyze clinical trials while overseeing statistical activities for programs and regulatory submissions. They will also manage day-to-day biostatistics operations, provide statistical consulting, and lead bid defense meetings with prospective clients.
The Feasibility Informatics Manager serves as a technical expert to lead clinical project feasibility strategies and support business development through data-driven insights. They are responsible for managing standalone feasibility projects, assessing risks, and coordinating with internal and external stakeholders to ensure optimal site selection and project delivery.
The Sales Representative is responsible for driving revenue growth by selling laboratory products and solutions to biotech, pharmaceutical, and academic research laboratories. They will manage the full sales cycle, develop territory business plans, and build strong consultative relationships with key decision-makers.
You will design and implement AI-driven solutions, including RAG techniques and agentic systems, to enhance clinical research and drug development. You will collaborate with cross-functional teams to integrate these AI features into a scalable, production-grade platform.
You will be responsible for building features from design to deployment while maintaining codebase health. Additionally, you will contribute to team processes and share knowledge through internal and external channels.
Lead the statistical strategy and execution for Phase I–III oncology trials while providing expert guidance on protocols and regulatory submissions. Mentor junior staff and drive continuous process improvement initiatives across clinical programs.
The Sales Development Account Manager is responsible for sourcing new sales opportunities through inbound lead qualification and outbound prospecting. They will collaborate with Business Development partners to manage territories, set appointments, and drive leads through the early stages of the sales process.
Lead end-to-end data management for complex, global clinical trials from study setup to database lock. Serve as the primary client contact while managing timelines, budgets, and cross-functional team performance.
Lead end-to-end data management for complex, global clinical trials from study setup to database lock. Serve as the primary client contact while managing timelines, budgets, and cross-functional team performance.
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Lead end-to-end data management for complex, global clinical trials from study setup through database lock. Serve as the primary client contact while managing timelines, budgets, and cross-functional team performance.
The Site Navigator I manages clinical trial start-up activities, including site identification, regulatory document coordination, and contract negotiations. They also perform in-house CRA responsibilities such as data validation, CRF review, and remote monitoring tasks.
You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Responsibilities include conducting site visits, resolving issues, and collaborating with cross-functional teams to ensure accurate data collection.
The Senior CRA will oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards. Responsibilities include conducting site visits, resolving issues, and collaborating with cross-functional teams to ensure accurate data collection.
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