2,264 Clinical Research jobs available for remote work from home. Apply for positions such as FSP - Sr. Regulatory and Start Up Specialist, Senior CRA- Remote/US, Senior Clinical Research Associate - Oncology - Northeast/Midwest (Remote), and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The specialist serves as the single point of contact for site activation activities, ensuring adherence to regulations and project timelines. Responsibilities include preparing regulatory documents, tracking approvals, and performing quality control on site deliverables.
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards. Lead monitoring tasks, conduct site visits, and collaborate with cross-functional teams for accurate data collection.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with informed consent and regulatory requirements.
Provide logistical and administrative support for site preparedness and remote monitoring in accordance with SOPs and regulatory guidelines. Assist CRAs with site management tasks, document collection, and the reconciliation of study data.
Develop and execute safety data review plans for clinical trials, focusing on AEs, SAEs, and laboratory data. Perform medical coding using MedDRA and WHODrug dictionaries while coordinating with data managers to ensure high-quality data collection.
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Oversees domestic and global Phase I clinical projects, managing scope, schedule, cost, and quality to meet client expectations. Leads cross-functional teams and handles risk assurance, regulatory documentation, and potential line management duties.
Provide logistical and administrative support for clinical trial site preparedness and remote monitoring activities. Assist CRAs with site management, document verification, and the coordination of study supplies and payments.
Provide logistical and administrative support for clinical trial site management and remote monitoring activities. Assist CRAs with site preparedness, document collection, and the reconciliation of study data in accordance with SOPs.
Provide logistical and administrative support for site preparedness and remote monitoring in accordance with SOPs and regulatory guidelines. Assist CRAs with site management tasks, document collection, and the reconciliation of study data.
Provide logistical and administrative support for clinical trial site preparedness and remote monitoring in accordance with SOPs. Assist CRAs with site management tasks, document collection, and the reconciliation of study data and payments.
The Clinical Development Trial Lead manages cross-functional teams to execute clinical trials on time, within scope, and within budget. They are responsible for trial enrollment strategies, risk mitigation, and maintaining the Trial Master File for inspection readiness.
The Senior CRA is responsible for investigative site management and monitoring activities throughout the clinical trial lifecycle for Oncology trials. Key duties include ensuring data integrity, subject safety, and maintaining a continuous state of inspection readiness.
Oversee the preparation, negotiation, and execution of clinical trial agreements and budgets for assigned studies. Coordinate contract management workstreams and serve as the primary escalation point for contract issues.
Provides scientific and medical guidance to operational teams and contributes expert input on RFPs, RFIs, and study execution strategies. Responsible for reviewing medical data and delivering therapeutic training materials.
Lead the daily operations, performance, and compliance of Clinical Research Specialist staff across designated health system accounts. Serve as the primary operational liaison to ensure high-quality service delivery and maintain strong customer relationships with health system partners.
Serves as the Database Administrator for Argus Safety, managing configuration, maintenance, and E2B reporting via gateway technologies. Provides technical leadership for system upgrades, case migrations, and ensures alignment with global regulatory requirements.
Manage and grow client relationships to drive revenue growth and ensure client satisfaction within the eClinical industry. Develop annual business plans and execute strategies to penetrate pharmaceutical, biotechnology, and medical device companies.
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Leads data management operations across a multi-site research network to ensure data quality, integrity, and operational visibility. Supervises a remote team of Data Entry Specialists and collaborates with clinical operations to optimize source documentation and data capture workflows.
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards. Lead monitoring tasks, conduct site visits, and collaborate with cross-functional teams for accurate data collection.
The Clinical Team Manager oversees all clinical operational and quality aspects of respiratory studies in compliance with ICH-GCP. This includes developing monitoring strategies, managing project financials, and leading clinical teams to ensure deliverables are met within contractual timelines.
Lead the initiation and activation of clinical trials by managing site-related essential document collection and review. Collaborate with internal teams and CROs to improve start-up metrics and ensure eTMF accuracy.
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards. Lead monitoring tasks, conduct site visits, and collaborate with cross-functional teams for accurate data collection.
Facilitate site start-up and activation by managing essential document collection and reviewing site-level Informed Consent Forms. Collaborate with internal teams and CROs to improve SSU metrics and ensure study timelines are achieved.
The role involves coordinating the setup and monitoring of clinical trials, ensuring accurate study status reports and documentation. It also requires maintaining strong relationships with stakeholders and ensuring compliance with regulatory requirements and patient safety.
The Clinical Risk Manager I will lead risk-based monitoring strategies, including the development of Integrated Quality Risk Management Plans and the identification of critical data and processes. They will serve as a subject matter expert to support cross-functional teams in mitigating protocol execution risks throughout the project life cycle.
The role involves managing and mentoring Clinical Team Managers to ensure the successful execution of clinical deliverables within assigned projects. It also requires overseeing budgeting, resource allocation, and the implementation of performance metrics for the clinical management group.
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Lead the initiation and activation of clinical trials by managing essential document collection and review. Collaborate with internal teams and CROs to improve start-up metrics and ensure eTMF accuracy.
Responsible for developing and writing scientific and technical content for study proposals and responding to RFIs. Coordinates with internal subject matter experts and external KOLs to ensure accurate, compelling, and compliant proposal delivery.
The MSL will execute field medical plans in France by engaging in scientific dialogue with healthcare professionals and cultivating relationships with Key Opinion Leaders. They will serve as a therapeutic expert and liaison between the company and clinical study sites to support medical education and congresses.
You will lead the planning, execution, and monitoring of complex clinical trials while ensuring adherence to regulatory requirements and project timelines. Additionally, you will collaborate with cross-functional teams to manage study plans, budgets, and resolve intricate operational challenges.
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