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.
Remote Clinical Research Jobs (1,598)
Tags = clinical-research
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.
Lead the preparation and maintenance of Clinical Trial Applications (CTAs) and Investigational New Drug (IND) applications. Oversee regulatory workstreams to ensure compliance with local and global requirements while providing strategic input to clinical study teams.
Lead and oversee clinical data programming activities across multiple trials to ensure quality and regulatory compliance. Coordinate data analysis delivery, develop programming strategies, and mentor team members in best practices.
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.
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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 clinical trial site management and monitoring activities to ensure compliance with ICH-GCP and regulatory requirements. Partner with clinical sites and cross-functional teams to support high-quality study execution and patient recruitment.
Lead the planning, execution, and delivery of clinical research projects to advance healthcare initiatives. Direct project management strategies to ensure quality, efficiency, and alignment with organizational business objectives.
Manage and process payments to clinical trial investigators while ensuring accuracy and compliance with contractual agreements. Collaborate with clinical and finance teams to resolve payment discrepancies and maintain detailed financial records for audits.
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 Scientific Advisor provides expert consultation to design electronic data collection solutions and translate clinical requirements into study strategies. They support sales and marketing efforts through bid defenses, protocol reviews, and the development of scientific content.
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.
The Coder Physician is responsible for abstracting and assigning accurate diagnosis and procedure codes from medical records for reimbursement and reporting. This includes maintaining a 95% quality rating and ensuring compliance with HIPAA and regulatory standards.
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.
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Coordinate project and programme management delivery for clinical trials, acting as the primary contact for sponsors. Manage 10-15 studies ensuring adherence to Good Clinical Practice and providing regular management reports.
Clinical Sales Specialist, Structural Heart - TEER (Hawaii / Bay Area, CA)
Abbott
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Full Time
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2 Weeks Ago
Abbott
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.
Sr Clinical Scientist
iRhythm Technologies, Inc.
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Full Time
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2 Weeks Ago
iRhythm Technologies, Inc.
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.
Clinical Research Associate II
Precision Medicine Group
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Full Time
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2 Weeks Ago
Precision Medicine Group
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.
Clinical Research Associate II
Precision for Medicine
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Full Time
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2 Weeks Ago
Precision for Medicine
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.
The Associate Director is responsible for developing and managing strategic relationships with Oncology and Hepatology sites to optimize clinical trial environments. This includes conducting environmental surveillance, driving site performance via KPIs, and implementing digital solutions to reduce cycle times.
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.
Senior Manager, Clinical Site Partner (Italy)
Summit Therapeutics
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Full Time
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2 Weeks Ago
Summit Therapeutics
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.
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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.
The Senior Project Coordinator manages administrative and coordination activities to keep clinical research projects organized. Key duties include maintaining timelines, managing Trial Master Files, and coordinating site training and documentation.
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.
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