2,268 Clinical Research jobs available for remote work from home. Apply for positions such as Contract Specialist - FSP - Italy, Manager Research Regulatory Affairs, Manager Research Regulatory Affairs, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Contract Specialist will negotiate clinical trial agreements, budgets, and payment terms while managing the contract lifecycle for site-related activities. They will collaborate with cross-functional teams to ensure compliance with regulatory requirements and facilitate timely study execution.
The Manager of Regulatory Affairs oversees all regulatory operations for site clinical operations and ensures full compliance with FDA and GCP guidelines. They are responsible for managing the regulatory department, developing compliance strategies, and coordinating relationships with industry sponsors and governmental auditors.
The Manager of Regulatory Affairs oversees all regulatory operations for site clinical operations and ensures full compliance with FDA and GCP guidelines. They are responsible for managing the regulatory department, developing compliance strategies, and fostering relationships with industry sponsors and government agencies.
The Section Head will lead the Chest Radiology department, overseeing diagnostic and treatment procedures while collaborating with multidisciplinary teams. The role involves participating in academic activities, including research, teaching, and the integration of AI and natural language processing technologies.
You will manage contract activities, including negotiating clinical trial agreements, budgets, and payment terms with assigned sites. Additionally, you will perform invoicing, reporting, and collaborate with internal teams to ensure study startup metrics and timelines are met.
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The Regulatory Affairs Specialist will plan, compile, and submit regulatory documentation while ensuring compliance with evolving global regulations. They will also act as a key point of contact for regulatory intelligence and provide strategic advice to project teams regarding submission processes.
The Project Manager is responsible for leading cross-functional teams to deliver clinical research projects on time, within budget, and to high quality standards. Key duties include developing detailed project plans, managing stakeholder expectations, and monitoring project progress to mitigate risks.
Perform monitoring and site management to ensure clinical studies adhere to protocols, regulations, and sponsor requirements. Manage site practices, including recruitment planning, regulatory submissions, and data integrity.
The Clinical Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol, GCP, and regulatory compliance. They also manage study-specific risks, oversee clinical team deliverables, and coordinate with functional leaders to meet study milestones.
The Business Intelligence Manager will drive strategic analytics and reporting solutions to support clinical research operations and leadership decision-making. Responsibilities include developing Power BI dashboards, ensuring data governance, and leading continuous improvement initiatives across the organization.
The Clinical Research Coordinator ensures oversight and compliance of system-wide clinical research activities for the Retrospective Core. They are responsible for study management, data collection, data integrity, and safeguarding participant privacy in accordance with regulatory standards.
The Contract Analyst will manage clinical trial site contracting, including negotiating budgets, payment terms, and clinical trial agreements. They will also oversee invoicing processes and collaborate with internal teams to ensure study startup metrics and timelines are met.
The specialist will facilitate site start-up activities, including essential document collection and review to ensure study timelines are met. They will also partner with internal teams and CROs to resolve activation delays and maintain accurate eTMF records.
The Clinical Team Manager is responsible for managing all clinical operational and quality aspects of allocated studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, monitor trial performance, and ensure compliance with ICH GCP and corporate policies throughout the study lifecycle.
The Clinical Business Analyst bridges scientific and technical teams to translate complex clinical study requirements into functional software solutions. They are responsible for documenting business requirements, managing system configurations, and supporting the full software development lifecycle including UAT and deployment.
The Senior Clinical Study Manager will lead end-to-end clinical trial execution, ensuring alignment with regulatory requirements, timelines, and quality standards. They will oversee study planning, vendor management, and cross-functional collaboration to drive program milestones and ensure data integrity.
The Senior Medical Project Coordinator manages and evaluates medical projects to ensure compliance, consistency, and optimal performance throughout the project lifecycle. They also serve as the primary point of contact for clinical project teams and monitor project financial status and operational risks.
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The Central Study Coordinator manages patient education, retention, and study matching by interpreting lab results and conducting virtual informed consent processes. They act as a virtual partner to participants, ensuring high-quality customer experience and accurate documentation in accordance with clinical research protocols.
The role involves administering clinical assessments to trial participants and evaluating the quality of assessments performed by other raters to ensure data reliability. You will provide feedback on methodology and scoring while maintaining accurate documentation for clinical trial activities.
The Clinical Research Associate will monitor clinical trial sites through on-site and remote visits while maintaining strong relationships with investigators and site staff. They are responsible for managing study documentation, ensuring compliance, and implementing corrective actions to maintain study integrity.
The role involves administering clinical assessments to trial participants and evaluating the quality of assessments performed by other raters to ensure data standardization. You will provide feedback on scoring techniques, manage documentation, and conduct remote interactions with participants and raters.
The Director of Operations is responsible for driving the growth, scalability, and operational consistency of the Remote Research Clinicians business. This role provides strategic leadership across client engagement, technology-enabled operations, and quality oversight to ensure delivery excellence.
The research data specialist is responsible for reviewing and abstracting medical records for research patients and entering clinical data into the database. They must ensure the quality, completeness, and timely entry of all data points.
The Clinical Study Manager oversees the planning, execution, and monitoring of clinical trials to ensure regulatory compliance and adherence to project timelines. They also collaborate with cross-functional teams and stakeholders to manage study budgets, resources, and resolve operational challenges.
The Senior Feasibility Specialist leads clinical research tasks by conducting in-depth feasibility assessments and evaluating site capabilities to ensure trial success. They collaborate with cross-functional teams to analyze data, prepare comprehensive reports, and provide mentorship to junior team members.
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.
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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 project teams.
The Senior Science Program Manager will orchestrate an international research portfolio in the UAE, ensuring alignment with Oura's strategic growth objectives. They will serve as a cross-functional hub, managing external partnerships and driving the execution of clinical and scientific initiatives.
Serve as the primary point of contact for investigational sites while conducting site visits to ensure compliance with ICH-GCP and regulatory standards. Manage site documentation, monitor patient safety, and oversee drug accountability to ensure high-quality clinical data.
You will conduct clinical trial monitoring activities, including site qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators and site staff while performing data reviews to maintain high-quality clinical documentation.
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