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University RetinaNew
Overview
The Clinical Research Assistant is responsible for recruiting and screening subjects and coordinating patient visits for clinical trials. They must collect accurate research data and ensure strict adherence to study protocols and GCP guidelines.
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Compensation
$21 - $24 / HOUR
Posted
New
Houston Retina AssociatesNew
UT Health San AntonioNew
Provide technical assistance for research projects focusing on recurrent pregnancy loss in humans. Responsibilities include conducting scientific experiments, interpreting clinical data, and performing limited administrative laboratory duties.
Salary not listed
UPMCNew
The Research Associate will execute research protocols for the ECHO Study, including recruiting participants and obtaining informed consent. They will conduct interviews, collect biospecimens, and assist with data cleaning and administrative tasks.
Johns Hopkins UniversityNew
The coordinator manages the administrative and logistical implementation of clinical research protocols to ensure validity of findings. Key duties include participant recruitment, consenting, data collection, and coordinating with the Institutional Review Board.
$17 - $30 / HOUR
University of Massachusetts Medical SchoolNew
The Research Nurse Coordinator I manages complex research protocols, ensuring adherence to GCP standards and regulatory requirements. They act as a primary liaison between clinical partners, investigators, and sponsors while overseeing patient care and data integrity.
The Research Associate provides operational support to the laboratory by performing defined research experiments under the direction of the Principal Investigator, ranging from basic tasks at Level I to independent project management and protocol development at Level IV. Responsibilities also include maintaining accurate records, assisting with data analysis, monitoring supplies, and ensuring compliance with all safety and institutional regulations.
The Research Associate provides operational support to the laboratory, performing research experiments focused on microbiota-metabolite-immune system crosstalk in the intestines using advanced techniques like flow cytometry, sequencing, and metabolomics. Responsibilities scale with rank, ranging from performing basic experiments and maintaining records to independently designing complex experiments, managing lab operations, and contributing to grant and manuscript writing.
University of Texas Medical Branch (UTMB)New
Provides professional nursing care for participants in oncology and hematology research studies while ensuring compliance with study protocols and federal regulations. Manages clinical study operations, including participant recruitment, informed consent, data collection, and regulatory documentation.
Provides professional nursing care for participants in oncology and hematology research studies while ensuring compliance with study protocols and federal regulations. Manages clinical study operations, including participant recruitment, data collection, and regulatory documentation.
The Clinical Research Coordinator manages human subject research protocols, including regulatory documentation, participant visits, and data collection. They ensure compliance with federal and institutional guidelines while supporting investigators with grant preparation and study reporting.
The Clinical Research Coordinator I is responsible for coordinating regulatory activities and managing data collection for research protocols. This includes obtaining consent from participants, scheduling study visits, and ensuring compliance with protocols.
UTHealth (University of Texas Health Science Center at Houston)New
Perform foundational laboratory procedures and translational research to support studies on lung and skin diseases. Responsibilities include maintaining mouse colonies, executing molecular biology protocols, and documenting experimental results.
PsychoGenics Inc.New
The candidate will support preclinical studies using rodent models by performing dosing, surgical nursing, and behavioral assessments. They are also responsible for tissue collection, data handling, and coordinating study execution.
The candidate will support preclinical studies using rodent models by performing dosing, surgical nursing, and behavioral assessments. They will also be responsible for tissue collection, data handling, and coordinating study execution.
Duke CareersNew
The coordinator will manage study start-up and close-out, recruit participants, and conduct clinical assessments. They are also responsible for administering neuromodulation treatments and collecting EEG and neuroimaging data.
$59,829 - $99,960 / YEAR
Perform technical duties including conducting physical, chemical, or biological tests and documenting results to support research activities. Responsibilities include setting up laboratory apparatus, preparing reagents, and maintaining equipment inventory.
$18 - $26 / HOUR
University of FloridaNew
Coordinates clinical research protocols by recruiting participants, managing informed consent, and ensuring regulatory compliance. Acts as a liaison between investigators, sponsors, and IRBs while managing study documentation and finances.
$53,000 - $57,000 / YEAR
Children’s Hospital of PhiladelphiaNew
Perform research protocols and experimental procedures focusing on the in vitro generation of red blood cells from induced pluripotent stem cells. Maintain laboratory equipment, manage supplies, and assist in the preparation of grants and journal articles.
$43,900 - $53,440 / YEAR
Children's Hospital of PhiladelphiaNew
Perform research protocols and experimental procedures focused on the in vitro generation of red blood cells from induced pluripotent stem cells. Maintain laboratory operations, including tissue culture, molecular biology procedures, and general lab maintenance.
