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Fortrea
Overview
The Research Nurse will deliver high-quality care to trial participants, monitor their well-being, and respond to emergencies while administering investigational compounds and performing study procedures like ECGs and venipuncture. Responsibilities also include collecting and processing biological samples and ensuring strict adherence and accurate record-keeping for clinical protocols.
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Compensation
Salary not listed
Posted
3 days ago
Perform clinical tasks including venipuncture, ECGs, and vital signs readings for healthy volunteers in Phase 1 clinical trials. Collect and process biological samples according to study protocols while maintaining a safe and efficient clinic environment.
5 days ago
K2 Staffing LLC
The Clinical Research Assistant supports clinical trial performance by managing candidate screening and maintaining accurate source documentation. They perform clinical tasks including phlebotomy and ECGs while ensuring strict adherence to study protocols and federal regulations.
10 days ago
Medpace, Inc.
Perform routine and esoteric clinical laboratory testing on blood, tissue, and body fluids following Standard Operating Procedures. Responsibilities include sample entry, instrument maintenance, reagent preparation, and participating in the validation of new methods.
Perform low, moderate, and high-complexity testing on blood, tissue, and body fluids. Collaborate with scientists to develop and validate new tests and methods for routine and biomarker testing.
TFS HealthScience
The Study Coordinator serves as the primary contact for sponsors, patients, and partners to ensure smooth study execution. Key duties include managing patient recruitment, coordinating communication with ethics committees, and overseeing regulatory compliance and audits.
The role is responsible for the operational conduct of assigned clinical studies, ensuring compliance with regulatory requirements and protocols. Key duties include study set-up, coordinating critical events, monitoring participant safety, and facilitating study planning meetings.
The role is responsible for the operational conduct of assigned clinical studies, ensuring compliance with regulatory requirements and protocols. Key duties include study set-up, coordinating critical events, and managing participant safety and eligibility.
The intern will assist with quality system documentation, record management, and audit preparation activities. They will also collaborate with QA staff to review data and support compliance initiatives.
Provide high-standard clinical care to healthy volunteers in Phase 1 clinical trials, ensuring participant safety and welfare. Responsibilities include administering investigational compounds, performing clinical procedures, and documenting adverse events according to study protocols.
12 days ago
Administer and interpret quantitative and qualitative psychometric tests for clinical trial participants focusing on neurodegenerative and mental health disorders. Ensure data collection adheres to study protocols, FDA guidelines, and Good Clinical Practice while coordinating with investigators and sponsors.
Florida Cancer Specialists
The Clinical Research Coordinator III is responsible for the successful implementation and ongoing site management of research studies under the supervision of the Principal Investigator. They also provide clinic coverage, mentor new research staff, and assist with assigned research projects.
17 days ago
Provide high-standard clinical care to healthy volunteers in Phase 1 clinical trials, ensuring participant safety and welfare. Responsibilities include administering investigational compounds, performing clinical procedures like venipuncture and ECGs, and documenting adverse events.
18 days ago
ICON plc
The Clinical Research Nurse provides direct clinical care to research participants and administers investigational products while monitoring safety. They also coordinate study procedures, ensure protocol compliance, and maintain accurate documentation of research data.
The Senior CRA is responsible for conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and data integrity. They also collaborate with site staff and contribute to the preparation of study documentation and clinical study reports.
The role involves conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. Additionally, the CRA will collaborate with site staff and perform data review to maintain high-quality clinical trial documentation.
You will oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice standards. This involves conducting site visits, collaborating with cross-functional teams, and providing training to site staff to ensure successful trial execution.
The Senior CRA oversees clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. They conduct site visits, manage data collection, and provide training to site staff to ensure successful trial execution.
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.
Coordinate and execute the screening and eligibility determination of volunteers for early phase clinical trials. This includes conducting clinical tasks like vitals and ECGs, obtaining informed consent, and maintaining participant data in databases.
24 days ago
