2,591 Clinical Research jobs available for remote work from home. Apply for positions such as Senior Informaticist – Health Informatics (Ontologist), Clinical Research Associate, Senior Clinical Research Associate - FSP - South West England, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Senior Informaticist will lead complex technical projects, manage biomedical ontologies, and ensure semantic consistency across clinical research data. They will also mentor junior staff and provide expert guidance on data architectures and standards to internal teams and clients.
The Clinical Research Associate is responsible for conducting monitoring visits to ensure data integrity, patient safety, and adherence to clinical study protocols. They also manage site documentation, maintain the Trial Master File, and ensure all activities comply with ICH/GCP guidelines and country-specific regulations.
The Senior Clinical Research Associate is responsible for the successful delivery of clinical studies at assigned investigator sites, including site management, monitoring, and study execution. They serve as the primary point of contact for sites to ensure high-quality data collection, patient safety, and regulatory compliance.
You will be responsible for reviewing, analyzing, and negotiating clinical trial contracts and vendor agreements to ensure regulatory compliance. Additionally, you will collaborate with cross-functional teams to mitigate risks and maintain accurate records within contract management systems.
You will assist in the coordination and administration of clinical trials while ensuring strict compliance with protocols and regulatory requirements. Additionally, you will manage essential study documentation and collaborate with cross-functional teams to facilitate smooth trial execution.
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The Regional Clinical Study Manager is responsible for the regional delivery of clinical studies, ensuring quality, adherence to timelines, and budget management. They lead the regional clinical operations team, oversee external vendors, and ensure compliance with regulatory standards and study protocols.
You will partner with clinical scientists to design and implement training and calibration strategies that ensure high-quality clinical endpoint assessments. Additionally, you will monitor clinician performance, provide coaching, and ensure all training documentation complies with regulatory standards.
The Regulatory and Start Up Specialist is responsible for managing site activation readiness, preparing clinical trial submission dossiers, and ensuring compliance with local and international regulations. They also facilitate communication between key project functions and maintain project trackers to ensure timely study initiation.
The specialist is responsible for the timely and high-quality activation of clinical trial sites, including the preparation of regulatory submission dossiers and management of site-level critical paths. They also facilitate communication between key project functions and ensure compliance with international and local clinical trial regulations.
The Regulatory and Start Up Specialist is responsible for managing site activation readiness, including the preparation and submission of clinical trial applications to regulatory authorities and ethics committees. They also coordinate essential document collection, maintain project trackers, and ensure compliance with international and local regulations throughout the study start-up phase.
The Regulatory and Start Up Specialist is responsible for the timely and high-quality activation of clinical trial sites, including the preparation and submission of regulatory dossiers to authorities and ethics committees. They also manage site-level critical paths, facilitate document translations, and ensure compliance with international and local regulations throughout the study lifecycle.
The Senior CRA is responsible for conducting onsite monitoring visits, managing clinical sites, and ensuring data quality and compliance with study protocols. They also act as a primary point of contact for stakeholders and support regulatory document preparation.
You will be responsible for conducting clinical trial monitoring activities, including site visits and ensuring protocol compliance and data integrity. Additionally, you will collaborate with investigators and site staff to facilitate study conduct and prepare essential study documentation.
The associate will serve as the primary contact for clients, managing the end-to-end process of licensing and translation for Clinical Outcome Assessments. They are responsible for preparing proposals, coordinating project activities, and ensuring high-quality delivery within established timelines and budgets.
The Senior Clinical Data Manager oversees all aspects of the clinical trial data management process, from study startup to database lock. They are responsible for managing project timelines, ensuring data quality, and coordinating with stakeholders and vendors.
The Senior Clinical Data Manager oversees all aspects of the clinical trial data management process, from study startup to database lock. They are responsible for managing project timelines, ensuring data quality, and coordinating with stakeholders and vendors.
The Site Contract Specialist manages the drafting, negotiation, and finalization of investigator contracts and budgets while ensuring compliance with company and client standards. They also coordinate with internal teams to align site startup activities with project timelines and provide mentorship to junior staff.
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The IRT Test Analyst is responsible for writing and executing test plans and use cases to ensure the functionality of IRT systems and project configurations. They also document system errors, track resolutions, and serve as a subject matter expert for software testing within clinical research projects.
Provides administrative and technical support to clinical research project teams, including coordinating project documents, records, regulatory materials, communications, and local payments. Supports reporting and data collection, resolves documentation findings, coordinates meetings and minutes, and assists with project management activities and study dashboards.
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 site staff and investigators while performing data review to maintain high-quality clinical documentation.
The Clinical Trial Manager III oversees the end-to-end delivery and operational execution of clinical research trials, ensuring adherence to budget, timelines, and quality standards. They lead site identification, regulatory submissions, and cross-functional team collaboration to maintain inspection readiness and data integrity.
The MSL will support GSK's hepatology clinical trials by facilitating scientific exchange with investigators and trial sites. They will also provide insights to internal teams regarding trial execution, operational challenges, and scientific feedback.
The Senior Clinical Research Associate is responsible for managing and overseeing assigned clinical study sites to ensure data quality, patient safety, and regulatory compliance. They also provide mentorship to junior team members and collaborate with clinical study teams to drive study milestones and process improvements.
Develop and implement strategic patient recruitment and retention plans to ensure clinical trials meet their timelines and milestones. Act as an expert consultant to project teams while managing vendor relationships and maintaining compliance with regulatory standards.
The Account Manager will serve as the primary point of contact for clients, managing relationships and coordinating clinical translation and linguistic validation projects. Responsibilities include developing proposals, managing budgets, and ensuring project delivery meets quality and timeline expectations.
Develop and execute patient-focused medical strategies for bone health therapies, including evidence generation, scientific engagement, lifecycle management, and medical communications. Build relationships with healthcare stakeholders, support clinical studies and governance activities, ensure regulatory and compliance standards, and contribute to medical planning and resource decisions.
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The IT Project Manager I provides technical project management and oversight for complex, cross-functional IT projects. They are responsible for managing project schedules, facilitating stakeholder communication, and ensuring project success criteria are met.
The Integrated Solution Strategy Director will partner with internal business units to design and deliver competitive, oncology-focused clinical research solutions. They will lead pre-award strategy, conduct risk assessments, and provide consultative guidance to sponsors to drive business growth.
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 stakeholders to ensure study compliance and participate in process improvement initiatives to enhance start-up efficiency.
The Senior Patient Recruitment and Engagement Lead will provide strategic leadership for global patient recruitment and retention across clinical trials. This role involves managing recruitment campaigns, overseeing vendor performance, and collaborating with cross-functional teams to ensure enrollment success and quality data collection.
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