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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
Potomac Healthcare SolutionsNew
The nurse practitioner or physician assistant will diagnose and treat veterans under the direction of a supervising physician while collaborating with a PACT team. Responsibilities include developing patient management plans, ordering diagnostic tests, and maintaining accurate medical records in compliance with VA guidelines.
Salary not listed
Mass General Brigham
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.
$29 / HOUR
2 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.
3 days ago
Potomac Healthcare Solutions
The Nurse Practitioner will diagnose and treat veterans under the direction of a supervising physician while collaborating with the PACT team to develop patient care plans. Responsibilities include performing diagnostic tests, managing patient records, and providing ongoing health maintenance and counseling.
Avera Health
Coordinates and implements research study protocols, including participant recruitment, screening, and data collection. Manages laboratory specimens and ensures compliance with FDA regulations and Good Clinical Practices.
$22 - $37 / HOUR
4 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.
6 days ago
Nevada System of Higher Education
The Research Assistant will recruit and enroll patients for clinical trials while ensuring adherence to all local, state, and federal research regulations. Responsibilities also include maintaining accurate study documentation, processing lab specimens, and assisting with IRB submissions and on-site sponsor visits.
$19 - $27 / HOUR
8 days ago
Evolution Research Group
The Clinical Research Coordinator manages the implementation of clinical trials, ensuring adherence to protocols and regulatory requirements. They are responsible for screening and enrolling subjects, maintaining accurate study records, and reporting adverse events under the direction of the Principal Investigator.
9 days ago
American Addiction Centers
Provides administrative and operational support to the Alzheimer's Disease Research Center, splitting time between administrative and clinical cores. Key tasks include managing patient appointments, maintaining research logs, and supporting regulatory and financial processes.
$22 - $33 / HOUR
11 days ago
ProHEALTH Medical Management
The Staff Nurse is responsible for the overall assessment, planning, implementation, and evaluation of patient care. This includes providing clinical nursing care and ensuring compliance with established regulations and standards.
13 days ago
Adams Clinical
The Clinician-Rater conducts structured clinical interviews, diagnostic evaluations, and standardized rating scales to assess psychiatric and neurological conditions. They work within a multidisciplinary team to determine participant eligibility and ensure high-quality data collection for clinical trials.
$90,000 - $120,000 / YEAR
Ora
The Clinical Research Coordinator I collects and organizes subject information during clinical study visits while ensuring protocol compliance. They perform technician-based tasks, manage study documentation, and collaborate with investigators to execute research directives.
The Clinical Research Coordinator I collects and organizes subject information during clinical study visits while ensuring protocol compliance. They perform technician-based tasks, manage study documentation, and collaborate with investigators and project managers.
Duke Careers
Coordinate and manage oncology clinical trials, including study start-up, recruitment, and long-term follow-up for breast and gynecologic studies. Provide direct clinical nursing care to research participants, including chemotherapy administration and adverse event monitoring.
$64,966 - $104,996 / YEAR
15 days ago
St. Elizabeth Healthcare
Coordinate clinical research studies by managing subject enrollment, data collection, and regulatory compliance. Collaborate with physicians to open new studies and ensure adherence to protocol and FDA guidelines.
16 days ago
St. Luke's University Health Network
The coordinator is responsible for the screening, enrollment, and coordination of clinical trials while ensuring compliance with protocol and federal regulations. Key duties include managing study documentation, performing study procedures, and coordinating data collection across departments.
24 days ago
Valor Healthcare, Inc.
The Mental Health LCSW provides clinical counseling, case management, and therapy services to veterans and their families within an outpatient clinic setting. They collaborate with the PACT team to develop patient care plans and maintain accurate clinical documentation in VISTA/CPRS.
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.
26 days ago
IRONWOOD PHYSICIANS,P.C.
Manages and coordinates all clinical and administrative aspects of conducting clinical trials in accordance with protocol guidelines and federal regulations. Acts as a liaison between investigators, sponsors, and the IRB while performing patient procedures and assessments.
28 days ago
