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The Ohio State UniversityNew
Overview
Provide support for clinical research studies within the Department of Internal Medicine, specifically in Gastroenterology, Hepatology, and Nutrition. Responsibilities include coordinating study implementation, recruiting participants, performing diagnostic testing, and managing research data.
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Compensation
Salary not listed
Posted
New
Fortrea
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.
2 days ago
Mass General Brigham
Prepares sterile and non-sterile products in adherence to USP and hospital policies while managing investigational prescriptions via the CTP system. Responsible for inventory management, temperature monitoring, and coordinating with study teams and sponsors for clinical trials.
$21 - $30 / HOUR
University of Iowa
Manage and support clinical trial regulatory activities for the Pediatric Department, including IRB submissions and documentation. Act as a back-up study coordinator to assist with subject visits, data entry, and protocol execution.
3 days ago
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
Avalo Therapeutics
The Clinical Trial Associate will support the planning, execution, and delivery of clinical trials in compliance with regulatory standards and internal SOPs. Responsibilities include tracking study progress, managing vendor relationships, and ensuring the quality and completeness of trial documentation.
7 days ago
Vanderbilt University Medical Center
Coordinate clinical trial protocols, patient consent processes, and the preparation of IRB and regulatory documents. Identify and recruit research subjects while managing data collection and lab specimen shipping.
Evolution Research Group
The Research Assistant will support clinical teams by performing patient assessments, including vitals and phlebotomy, and managing study documentation. They are also responsible for data entry, specimen processing, and maintaining lab kit inventory in compliance with FDA and GCP regulations.
9 days ago
UT Health San Antonio
Responsible for assisting with the administration, organization, and implementation of clinical trial operations and systems management. The role involves performing technical reviews of research protocols, funding agreements, and billing processes within Neurosurgery and Neurocritical Care.
11 days ago
Rapport Therapeutics
The Senior Clinical Trial Associate manages clinical study documentation, including the Trial Master File, to ensure inspection readiness and compliance with ICH-GCP standards. They also support the trial team with administrative tasks, vendor invoice tracking, and the preparation of essential study-related documents.
$90,000 - $110,000 / YEAR
Cincinnati Children's
The role involves managing clinical trial conduct, including participant recruitment, specimen collection, and ensuring adherence to study protocols and regulatory requirements. It also requires maintaining accurate documentation, performing data management tasks, and serving as a liaison between investigators, sponsors, and clinical teams.
$56,784 - $62,150 / YEAR
15 days ago
Stanford Health Care
Provide hands-on, evidence-based nursing care to patients in inpatient clinical trials, including assessment, planning, and implementation of care. Coordinate with healthcare teams and educate patients and families to manage care and prevent complications.
$96 - $111 / HOUR
16 days ago
ICON plc
You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. This includes conducting site visits, collaborating with cross-functional teams, and providing training to site staff to ensure successful trial execution.
17 days ago
Crinetics Pharmaceuticals
The CTA supports the study team by executing study activities according to protocols and regulatory guidelines across investigator sites. Key duties include maintaining the Trial Master File, coordinating regulatory documents, and assisting with project management tasks from inception to database lock.
$70,000 - $87,000 / YEAR
21 days ago
University Hospitals
Coordinate and implement clinical research studies in GI while providing safe, age-specific nursing care to participants. Manage regulatory documentation, recruit participants, and ensure compliance with GCP and sponsor guidelines.
23 days ago
HUTCHINSON CLINIC P A INC
Coordinate clinical trial protocols including study initiation, recruitment, and regulatory compliance. Act as a liaison between providers, patients, and study representatives while managing medical documentation and patient visits.
Coordinate clinical trial protocols including study initiation, recruitment, and regulatory compliance. Act as a liaison between providers and patients while managing medical documentation and performing phlebotomy.
Baptist Health System, Inc.
The Research Assistant supports clinical trials by conducting literature reviews, collecting and analyzing study data, and managing patient recruitment. Additionally, they handle project administration, including budget monitoring, meeting minutes, and patient follow-up calls.
Responsible for assisting with the administration, organization, and implementation of clinical trial operations and systems management. Provides technical reviews of research protocols, funding agreements, and billing processes.
Baptist Health South Florida
The Research Associate 3 will be responsible for collecting, analyzing, and interpreting collected data. They will adhere to Baptist Health South Florida guidelines when presenting research outcomes and ensure high-quality research is performed.
$58,494 - $76,043 / YEAR
26 days ago
