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Arizona Liver HealthNew
Overview
Coordinate clinical research trials by recruiting participants, performing clinical procedures like phlebotomy and vitals, and managing study data. Ensure strict adherence to regulatory guidelines, maintain study documentation, and collaborate with sponsors and internal staff.
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Compensation
$28 - $36 / HOUR
Posted
New
ICON plc
The Sr. CRA is responsible for managing investigative sites and performing monitoring activities throughout the clinical trial lifecycle to ensure data integrity and subject safety. Key duties include conducting site visits, managing essential documents, and ensuring compliance with protocols and regulatory standards.
$110,520 - $138,150 / YEAR
2 days ago
American Addiction Centers
Coordinates clinical and administrative aspects of sponsored clinical trials, including subject recruitment, enrollment, and data collection. Acts as the primary liaison between sponsors and investigators while ensuring protocol adherence and regulatory compliance.
$31 - $46 / HOUR
IQVIA
The intern supports the preparation, documentation, and management of investigational products for clinical trials under pharmacist supervision. Key duties include managing drug accountability logs, dispensing medications per protocol, and ensuring regulatory compliance with FDA and IRB standards.
$33,000 - $82,600 / YEAR
Cleveland Clinic
Oversee the implementation and conduct of human subject research projects within the Heart, Vascular & Thoracic Institute. Perform nursing tasks including patient assessments, care plan development, documentation, and regulatory compliance.
Salary not listed
3 days ago
OneOncology
As the Research Nurse, you will screen, enroll, and follow study subjects, ensuring protocol compliance and monitoring. You will also be responsible for source documentation, recording adverse events, and dispensing investigational products.
University of Iowa
Provide direct nursing care and administer investigational treatments for Phase I-IV clinical trials. Collaborate with medical staff to ensure participant safety and strict adherence to research protocols.
4 days ago
Mid-Atlantic Permanente Medical Group PC
The Clinical Research Nurse coordinates the clinical trial study process, including patient recruitment, informed consent, and protocol-required assessments. They also ensure regulatory compliance by preparing IRB submissions and maintaining accurate study documentation throughout the lifecycle.
$79,370 - $99,213 / YEAR
The technician will be responsible for entering concomitant medications, preparing investigational products according to protocol, and compounding IV and oral agents adhering to USP standards. Key duties also involve managing drug inventory documentation and providing administrative support for audits and SOP development.
4 C Medical Technologies
This role involves developing, coordinating, and administering the logistical aspects of clinical trials in compliance with GCP, GDP, and SOPs, acting as a key communication point between staff, sites, and vendors. Key duties include overseeing trial operations, managing site documentation, corresponding with study sites regarding subject progress and queries, and coordinating adverse event information.
$75,000 - $95,000 / YEAR
6 days ago
Headlands Research
The Laboratory Technician performs specimen collection, processing, documentation, and shipment for clinical trials in compliance with GCP and study protocols, while also assisting with vital signs, ECGs, and maintaining laboratory equipment and cleanliness. Responsibilities also include accurate data recording, resolving data queries, monitoring lab inventory, and supporting study preparation activities.
$22 - $26 / HOUR
Cedars-Sinai
The Clinical Research Coordinator independently manages study coordination, including patient screening, informed consent, and data collection. They ensure compliance with federal and local regulations while maintaining accurate source documents and reporting study progress.
$27 - $42 / HOUR
Baptist Health System, Inc.
Conduct all aspects of clinical trials while ensuring compliance with local and federal regulations. Maintain Good Clinical Practice (GCP) standards to ensure subject safety and the validity of study data.
8 days ago
The Research Nurse Coordinator oversees the implementation and conduct of human subject research projects while ensuring adherence to protocols. They perform nursing assessments, manage regulatory documentation, and serve as a liaison between the research team and study participants.
The CRC manages Phase II-IV clinical studies from initiation to close-out, ensuring compliance with FDA and GCP guidelines. Key duties include conducting subject visits, managing recruitment, and maintaining accurate clinical documentation.
Visionary Ophthalmology
The coordinator manages day-to-day activities for ophthalmology clinical trials, including subject visits and regulatory compliance. They are responsible for data entry, maintaining study binders, and communicating with sponsors and CROs.
$25 - $30 / HOUR
Evolution Research Group
The Psychometric Rater is responsible for administering and scoring clinical tests and managing data collection for clinical trials. They collaborate with researchers to ensure strict adherence to study protocols, ethical guidelines, and FDA regulations.
$30 / HOUR
9 days ago
The Psychometric Rater is responsible for administering and scoring tests for clinical trial participants while ensuring strict adherence to study protocols and ethical guidelines. They collaborate with researchers to collect accurate data and manage participant documentation under the direction of the Principal Investigator.
$34 / HOUR
The Clinical Research Coordinator manages the implementation of clinical trials, including subject screening, enrollment, and the administration of study procedures. They ensure all activities comply with FDA regulations, GCP guidelines, and company SOPs while maintaining accurate study documentation.
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.
