2,257 Clinical Research jobs available for remote work from home. Apply for positions such as Clinical Education & Product Coordination Associate - Regional, ES, Clinical Research Associate II or Sr- Argentina, Solution Sales Specialist 3, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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Provide in-person customer support and technical training for Fujifilm's Endoscopy equipment during regional hands-on courses. Manage equipment logistics, including setup, troubleshooting, and maintenance, while identifying process improvements for efficiency.
Monitor clinical trial sites through on-site and remote visits while maintaining strong relationships with investigators. Ensure study integrity by managing documentation and keeping sites audit- and inspection-ready.
Drive new and expansion revenue for digital marketing offerings targeting hospital and health system clients across the West Coast. Partner with Account Directors to identify growth opportunities and deliver data-driven solutions that improve service line performance.
The MSL provides clinical and product education to healthcare providers to drive the adoption of molecular tests for breast cancer. They manage relationships with Key Opinion Leaders and stimulate investigator-initiated studies to generate real-world evidence.
Act as the primary scientific resource for Key Opinion Leaders and healthcare practitioners to educate them on ImmunityBio products and disease states. Facilitate clinical research, gather field insights, and implement medical affairs strategic plans within the Northeast region.
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The Oncology Data Specialist is responsible for abstracting cancer cases from electronic medical records into registry software and ensuring compliance with state and national reporting standards. Duties include performing case finding, follow-up, and resolving data edits prior to submission to the NCDB and State Central Registry.
Monitor the progress of clinical studies at investigative sites or remotely to ensure trials are conducted according to protocol. Ensure all recording and reporting comply with SOPs, ICH-GCP, and applicable regulatory requirements.
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
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 to ensure accurate data collection.
The EDC Specialist is responsible for accurate and timely data entry into clinical trial systems to support sponsor-facing work. They must maintain data quality, follow structured operational workflows, and communicate effectively with team members.
The Senior Clinical Data Scientist will act as the primary data architect for a large-scale commercial real-world evidence registry. They are responsible for designing EHR data extraction pipelines and transforming heterogeneous clinical data into analysis-ready datasets.
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 to ensure accurate data collection.
Engage oncology KOLs and investigators to facilitate collaborative external research, including investigator-initiated trials and real-world data studies. Serve as a scientific liaison between internal data scientists and external researchers to manage study workflows and medical writing.
Responsible for the timely preparation and submission of comprehensive safety reports, including PSURs and ICSRs. The role involves conducting data analysis to assess pharmaceutical safety profiles and collaborating with cross-functional teams.
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Responsibilities include ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
Provide clinical and sales support by training interventional cardiologists and catheter lab staff on Structural Heart products. Offer technical support during medical procedures and collaborate with Territory Managers to ensure positive patient outcomes.
Lead the scientific aspects of clinical research projects, including study design, analysis, and evidence dissemination for cardiac health solutions. Collaborate with cross-functional teams to develop clinical strategies and regulatory documentation to support market clearance and product innovation.
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Monitor and manage the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Coordinate all necessary activities for study setup, including identifying investigators and preparing regulatory submissions.
The CRA II will monitor clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Responsibilities include coordinating study setup activities, identifying investigators, and managing regulatory submissions.
Lead strategic oncology drug development program design and protocol development for solid tumors and hematologic malignancies. Serve as a scientific partner and trusted advisor to senior industry stakeholders while leading proposal development and bid defense activities.
The Coder ER reviews medical records to assign accurate diagnosis, procedure, and charge codes for reimbursement and statistical analysis. They are responsible for maintaining patient confidentiality and ensuring compliance with regulatory and accreditation standards.
Lead the operational execution of Phase I–III oncology clinical trials across Europe, serving as the primary point of contact for clinical sites. Drive site selection, activation, and recruitment while ensuring high standards of performance and quality throughout the study lifecycle.
Conduct scientific and regulatory reviews to evaluate the safety and effectiveness of new ophthalmic devices for the FDA. Prepare comprehensive memos and recommendations regarding submission clearance, approval, or disapproval for various medical device actions.
Lead complex enterprise client implementations from kickoff through deployment, serving as a trusted advisor to senior stakeholders. Coordinate with cross-functional teams to translate business requirements into technical specifications and ensure successful project execution.
The Coder Physician reviews medical records to assign accurate diagnosis, procedure, and charge codes for reimbursement and quality evaluation. They are responsible for abstracting clinical information from various medical records while maintaining strict patient confidentiality and HIPAA compliance.
Lead end-to-end data management for complex global clinical trials from setup to database lock. Serve as the primary client contact while overseeing data reconciliation, budgets, and the mentoring of junior staff.
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Provide expert consultation on RTSM and DHT study design, translating complex requirements into functional project specifications. Manage the delivery of project deliverables while collaborating with stakeholders and external clients to mitigate risks.
Independently lead global clinical projects within the Auto Immune area, managing budgets, scope, and cross-functional teams. Serve as the primary point of contact for clients and oversee all functional areas including data management, safety, and biostatistics.
Independently lead global clinical projects within the Auto Immune area, managing budgets, scope, and cross-functional teams. Serve as the primary point of contact for clients and oversee all functional areas including data management, safety, and biostatistics.
Independently lead global clinical projects within the Auto Immune area, managing budgets, scope, and cross-functional teams. Serve as the primary point of contact for clients and oversee all functional areas including data management, safety, and biostatistics.
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