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M3USA
Overview
The Clinical Research Assistant supports daily clinical trial activities, ensuring protocol compliance and data quality under the guidance of site leadership. Key duties include managing clinical supplies, performing phlebotomy, and documenting participant data in source records and EDC systems.
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Compensation
Salary not listed
Posted
17 days ago
The Clinical Research Coordinator manages daily clinical trial activities and supports the Principal Investigator in the conduct of studies. Key duties include screening participants, maintaining documentation, and ensuring compliance with research protocols and laws.
$30 - $40 / HOUR
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily clinical trial activities under the guidance of site management and the Principal Investigator. Essential duties include assisting the Investigator with participant screening, maintaining documentation, collecting and entering data, and overseeing other research staff.
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily activities of clinical trials under the guidance of site management and the Principal Investigator. Essential duties include assisting investigators with participant screening, maintaining documentation, mentoring staff, and ensuring all activities comply with research protocols and regulations.
West Cancer Center
Manage oncology patients in pharmaceutical-sponsored clinical trials, including screening, enrollment, and ongoing monitoring. Act as a liaison between the research team and clinical staff to ensure protocol compliance and patient safety.
21 days ago
The Clinical Research Coordinator manages daily clinical trial activities, including screening participants and maintaining essential study documentation. They ensure all activities comply with research protocols, laws, and regulatory requirements while supporting the Principal Investigator.
$25 - $35 / HOUR
University of Maryland Medical System
The role involves coordinating clinical research trials in radiation oncology, including protocol submission, patient recruitment, and data management. The coordinator acts as a liaison between sponsors, investigators, and review boards to ensure regulatory compliance and study integrity.
24 days ago
Baptist Health South Florida
The Nurse Research Coordinator supports the Clinical Research staff by coordinating and administering clinical study protocols in cooperation with the Principal Investigator. This role includes ensuring compliance with regulatory requirements and maximizing subject participation in cardiovascular research protocols.
27 days ago
OneLegacy
The Donor Information Coordinator is responsible for reviewing and completing tissue donor case files to ensure accuracy and regulatory compliance. This includes coordinating with hospitals, coroners, and processors to obtain necessary medical documentation and updating donor databases.
$46,675 - $67,683 / YEAR
1 month ago
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily clinical trial activities under the guidance of site management and the Principal Investigator. Essential duties include assisting the investigator with participant screening, maintaining documentation, and ensuring all activities comply with the research protocol and regulations.
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily activities of clinical trials under the guidance of site management and the Principal Investigator. Essential duties include assisting the investigator with screening, maintaining documentation, collecting and entering data, and mentoring junior staff.
UCSF
The Clinical Research Coordinator supports the management of investigator-sponsored research studies by maintaining protocol files, collecting data, and ensuring compliance with federal and institutional regulations. They also assist the research team with participant enrollment, survey administration, and project management tasks.
$38 - $61 / HOUR
HonorHealth
The Clinical Research Nurse coordinates and executes complex research protocols while providing high-quality, evidence-based nursing care to patients. They collaborate with multidisciplinary teams to ensure regulatory compliance, patient safety, and accurate data collection throughout the research process.
The Sterile Processing Technician is responsible for the decontamination, wrapping, and sterilization of instruments used in organ, eye, and tissue recovery. They also perform quality control releases and maintain the cleanliness and inventory of the central supply areas.
$43,680 - $53,955 / YEAR
OneOncology
This role involves assisting with various clinical research activities under mentorship, including screening potential subjects for eligibility against trial criteria and managing informed consent records. The coordinator will also be responsible for procuring, processing, and shipping biospecimens according to protocol and regulations.
2 months ago
ImmunityBio, Inc.
The Field Monitor will support clinical research teams by providing training, interpreting protocols, collecting and reviewing documents, and ensuring the efficient conduct of clinical studies. Key functions include developing training materials, serving as a Subject Matter Expert for sites, overseeing essential document collection, and managing investigational product supply.
$54 - $60 / HOUR
CenExel
The coordinator ensures the highest standards of data quality and participant safety are maintained, along with adherence to protocols, SOPs, and regulatory guidelines. This involves assisting the QA Manager, reviewing various study documents for trends, and performing ongoing quality reviews of study records and documentation.
