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UVA HealthNew
Overview
Coordinate oncology clinical trials by recruiting, screening, and enrolling participants while ensuring protocol compliance and high-quality data collection. Maintain accurate documentation and collaborate with multidisciplinary research teams to support the advancement of cancer research.
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Compensation
$28 - $81,500 / HOUR
Posted
New
Mass General Brigham
The Clinical Research Coordinator manages day-to-day operations of clinical research studies, including participant recruitment, data collection, and study visit coordination. They ensure protocol compliance and handle regulatory documentation and IRB submissions.
$29 / HOUR
2 days ago
ICON plc
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. They ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
$91,336 - $114,170 / YEAR
The Clinical Research Coordinator supports oncology clinical trials by enrolling eligible patients and scheduling all protocol-mandated tests. Responsibilities include coordinating patient appointments, processing tissue and blood samples, and maintaining communication with enrolled participants.
The coordinator will assist with clinical research studies by recruiting, evaluating, and consenting patients, collecting and organizing patient data, and scheduling study visits. Key duties also involve performing clinical tests like phlebotomy and EKGs, and maintaining study documentation and data integrity.
$20 - $29 / HOUR
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.
Salary not listed
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
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.
3 days ago
IQVIA
The Clinical Nurse is responsible for ensuring protocol compliance, managing clinical trial patients through assessment, documentation, and coordination of care, and adhering to all applicable regulations and institutional policies. This role involves effective communication with the interdisciplinary team, patient education, and accurate management of study-related procedures and documentation.
$62,700 - $156,700 / YEAR
Ascension
Coordinate administrative and clinical aspects of multiple oncology research projects, including participant recruitment and monitoring. Collaborate with investigators and sponsors to ensure protocol compliance and manage IRB documentation and audits.
4 days ago
Ann & Robert H. Lurie Children's Hospital of Chicago
This role coordinates and manages the initiation and regulatory compliance of clinical research studies, including preparing documents, managing study conduct across departments, and overseeing all aspects of clinical research visits. Responsibilities also include managing participant engagement, collecting specimens, recording data, assisting with financial aspects, and participating in investigator meetings.
$49,920 - $81,619 / YEAR
6 days ago
Headlands Research
Lead and oversee clinical trials, ensuring compliance with protocol requirements and regulatory standards. Provide leadership and mentorship to site staff while fostering a culture of inclusivity and professionalism.
University of Virginia
The coordinator will recruit, screen, consent, and enroll participants in oncology clinical trials while building relationships with patients and collecting high-quality data at study visits. Key duties involve maintaining accurate documentation, processing lab specimens, tracking adverse events, and ensuring strict protocol and regulatory compliance.
$33 - $92 / HOUR
7 days ago
Vail Health Hospital
The Clinical Research Coordinator manages clinical trials by ensuring patient safety, regulatory compliance, and accurate data collection. They coordinate patient recruitment, maintain study documentation, and facilitate communication between investigators, sponsors, and clinical staff.
$32 - $44 / HOUR
Coordinate oncology clinical trials by recruiting, screening, and enrolling participants while ensuring protocol compliance and high-quality data collection. Maintain accurate documentation and collaborate with multidisciplinary teams to support the advancement of innovative cancer research.
9 days ago
The coordinator will recruit, screen, consent, and enroll participants across multiple cancer clinical trials while building relationships with study participants. Key duties include coordinating study visits, collecting high-quality data, maintaining accurate documentation, processing specimens, tracking adverse events, and ensuring protocol compliance.
$28 - $82 / HOUR
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.
Key responsibilities involve preparing and administering specialized therapies, including IV infusions, monitoring study participants, and thoroughly documenting all clinical activities to support operational and clinical objectives. The role also requires conducting intake procedures, performing cognitive assessments, and maintaining clear communication to ensure participant safety and protocol compliance.
Vanderbilt University Medical Center
The Research Nurse Specialist 2 maintains the integrity and quality of clinical research trials, planning recruitment, managing enrollment, and ensuring protocol compliance under occasional guidance. Key duties include preparing research proposals, performing administrative tasks, utilizing nursing skills for procedures, and observing/reporting adverse events.
10 days ago
Avera Health
The Clinical Research Coordinator is responsible for daily clinical trial activities, including patient recruitment, screening, and enrollment. They also manage study data, conduct clinical assessments, and ensure compliance with research protocols and regulatory requirements.
$25 - $46 / HOUR
14 days ago
