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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
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
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.
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.
7 days ago
Headlands Research
Support clinical trial execution by conducting patient recruitment through outbound calls and assisting with subject screening and enrollment. Collect vital signs and document study data in electronic systems while ensuring compliance with study protocols.
9 days ago
Glaukos
The CRA is responsible for assessing, training, and monitoring clinical research sites to ensure data integrity and protocol compliance. This includes conducting site visits, managing investigator relationships, and overseeing the accountability of investigational products.
$73,600 - $85,000 / YEAR
Beth Israel Lahey Health
The nurse will support clinical research trials by collaborating with multidisciplinary teams to implement protocols and monitor patient data. They will also provide direct patient care, including symptom management and recruitment for various oncology studies.
$36 - $79 / HOUR
10 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.
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
Care Access
Perform clinical tasks including venipuncture and biospecimen processing to support clinical trials. Handle administrative duties such as participant scheduling, data entry, and maintaining site logs.
$24 - $38 / HOUR
13 days ago
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
The role involves providing primary telephone coverage to liaise with clinical sites and participants for a large randomized clinical trial. Responsibilities include conducting phone interviews, tracking participants, and ensuring recruitment goals are met while maintaining detailed documentation.
$20 - $29 / HOUR
16 days ago
ICON plc
The Medical Research Associate is responsible for greeting clinical research volunteers and performing vital sign assessments and phlebotomy procedures according to study protocols. They also provide personalized care to study subjects and ensure their comfort throughout the research process.
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
Ann & Robert H. Lurie Children's Hospital of Chicago
The coordinator supports the GROWTH study by managing regulatory documents, recruiting eligible subjects, and collecting and processing specimens. They are also responsible for data entry into electronic platforms and coordinating study visits and reimbursements.
$46,280 - $75,670 / YEAR
24 days ago
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
Thermo Fisher Scientific
The Clinical Trial Coordinator supports the planning and execution of clinical studies, focusing on day-to-day activities and regulatory inspection readiness. They collaborate with study teams, CROs, and internal departments to manage study documentation and clinical trial systems.
27 days ago
Olema Oncology
Provide administrative and operational support to clinical teams for in-house and outsourced trials. Manage study documentation, vendor relationships, and investigator site communications to ensure trial execution.
$110,000 - $120,000 / YEAR
