Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
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.
Quick view →
Compensation
Salary not listed
Posted
3 days ago
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.
10 days ago
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
The role involves balancing clinical patient care with a strong focus on Phase I clinical research as a Principal Investigator. Responsibilities include supporting study development and collaborating with internal colleagues and external referring physicians.
1 month ago
The role involves collecting, processing, and shipping biological specimens for early-phase clinical trials. Additionally, the technician is responsible for maintaining lab equipment, managing inventories, and ensuring a safe, compliant work environment.
The role involves utilizing clinical skills and judgment to provide high standards of care in clinical research, including accurately performing vital signs, ECGs, collecting and processing biological samples, and monitoring participant compliance with meals.
K2 Staffing LLC
The Sub Investigator ensures adherence to clinical trial protocols and federal regulations while protecting the rights and welfare of study subjects. They are responsible for managing the medical care of participants and maintaining the integrity of the data generated at the site.
Medpace, Inc.
Assist scientists in preparing protocols, methods, and reports for clinical studies. Compile and review data from instruments and the Watson-LIMS database to ensure accurate documentation.
The associate will manage sponsor audits and regulatory inspections (FDA, EMA, MHRA), facilitate QA relationships with external clients, and conduct inspection readiness activities for Medpace stakeholders. Key duties include facilitating onsite audits, reviewing audit responses, managing inspection backrooms, and providing guidance to study teams during inspections.
The Clinical Trial Associate supports Trial Master File (TMF) oversight by ensuring all documents meet established quality standards, which involves managing electronic filing systems, tracking, maintaining, and performing quality checks on documents. This role also requires communication with internal associates globally regarding document errors and preparing documents for shipment.
2 months ago
MESO SCALE DIAGNOSTICS, LLC.
The technician is responsible for performing preventative maintenance on laboratory equipment and managing the receipt, verification, and storage of clinical samples. They must also document all activities in compliance with GLP/GCLP standards and maintain accurate sample tracking logs.
$45,500 - $66,000 / YEAR
The Clinical Nurse Study Coordinator is responsible for the accurate administration of medications, monitoring of adverse events, and performing clinical procedures according to study protocols. They also collaborate with project managers and investigators to ensure operational flow and data integrity.
