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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
2 days ago
Sonic Healthcare USA
The Clinical Research Coordinator is responsible for the identification, retrieval, and processing of archived biological samples for pre-clinical research. They must maintain accurate documentation and ensure all activities comply with federal regulations and IRB guidelines.
4 days ago
UTHealth Houston
Support gynecologic oncology research by assisting with study development, data collection, and analysis. Coordinate laboratory and clinical research activities while maintaining accurate documentation and a safe work environment.
8 days ago
Evolution Research Group
The Patient Care Technician oversees the care of clinical trial subjects and performs medical procedures including blood collection and ECGs. They are responsible for sample processing, documentation, and maintaining a safe environment in accordance with regulatory guidelines.
9 days ago
The Patient Care Technician oversees the care of clinical trial subjects and performs medical procedures including blood collection and ECGs. They are responsible for maintaining a safe environment and ensuring compliance with GCP and ICH guidelines.
The role involves supporting gynecologic oncology research through study development, data collection, and the coordination of laboratory and clinical activities. Key duties include performing experiments, maintaining accurate documentation, and managing laboratory supplies.
The Unit Clinician assists with clinical trial execution by performing procedures such as venipuncture, ECGs, and biological sample collection. They are responsible for dispensing medications, documenting subject data, and maintaining a safe, compliant work environment according to study protocols.
Headlands Research
Support clinical trials by preparing study documents, recruiting participants, and conducting patient-facing procedures like vital signs and phlebotomy. Manage study data entry in EDC and CTMS systems while ensuring compliance with FDA and GCP guidelines.
$22 - $27 / HOUR
PsychoGenics Inc.
Perform daily husbandry, sanitation, and maintenance of colony rooms and animals within the vivarium. Oversee documentation, inventory monitoring, and the safe disposal of laboratory medical and chemical waste.
20 days ago
Quotient Sciences
The primary duties involve collecting biological samples, performing phlebotomy, recording vital signs, and ensuring all study data collection adheres to Good Clinical Practice (GCP) standards for participant safety.
21 days ago
Arkansas Children's Hospital
The Research Assistant Clinical supports various clinical trials and research studies by managing data collection, participant records, and recruitment. They are responsible for adhering to study protocols and collaborating with the Principal Investigator to ensure regulatory compliance.
24 days ago
ThedaCare
The Clinical Research Specialist coordinates clinical trials by screening patients for eligibility and managing the informed consent process. They are responsible for accurate data collection, maintaining source documents, and ensuring compliance with federal and institutional regulations.
25 days ago
Community Veterinary Partners
The Veterinary Technician assists veterinarians during examinations and surgeries, collects and processes biological samples, and administers medications. They also educate pet owners on animal care and maintain cleanliness in the hospital environment.
28 days ago
Sanford Health
Provide technical assistance in histology and clinical laboratories, including preparing tissues for examination and processing biological specimens. Responsibilities also include equipment maintenance, stocking supplies, and training new employees.
$23 - $36 / HOUR
1 month ago
CentraState Healthcare System
The Research Nurse oversees and directs the clinical course of research participants in clinical trials under the direction of the principal investigator or manager, ensuring strict adherence to local and federal laws and regulations. Key duties involve study implementation, subject recruitment, enrollment, accurate documentation, and acting as the liaison between the sponsor and physician regarding protocol activities.
$48 - $82 / HOUR
University of Chicago
Conduct comprehensive clinical research assessments and manage participants in studies focused on Alzheimer's and dementia. Collaborate with multidisciplinary teams to ensure protocol adherence, regulatory compliance, and high-quality data collection.
$128,000 - $163,500 / YEAR
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.
Tufts Medicine
The role supports research on babesiosis by developing protein-based vaccines and testing treatment compounds. Responsibilities include performing lab techniques, collecting data, and maintaining records in accordance with IRB requirements.
$43,888 - $53,338 / YEAR
Health Haven
Oversee day-to-day coordination of clinical trials, ensuring protocol adherence and high-quality data collection. Coordinate with investigators and sponsors while managing patient recruitment and regulatory compliance.
$25 - $35 / HOUR
