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ICON plc
Overview
The Lab Analyst I will perform and report routine and special laboratory tests on clinical trial specimens to support subject safety and protocol requirements, while also analyzing results for accuracy and managing laboratory instrumentation. Responsibilities include performing specimen processing, running quality controls, calculating and verifying results using LIS/eSource, and notifying the Principal Investigator of critical values.
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Compensation
Salary not listed
Posted
3 days ago
Valley Healthcare System Inc
The Certified Nurse Practitioner will obtain comprehensive health and psychosocial assessments, implement treatment regimens for acute and chronic patients, and order/interpret routine diagnostic tests according to established protocols. Responsibilities also include developing health promotion plans, co-managing care with physicians, and performing specialized gynecological assessments and treatments.
$97,139 - $121,424 / YEAR
11 days ago
University of Miami
The coordinator manages the day-to-day operations of clinical research protocols from initiation to close-out, ensuring participant safety and adherence to guidelines. Key duties include recruiting participants, collecting data, processing specimens, and maintaining regulatory documentation.
The Clinical Research Coordinator 2 assists in planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies, managing day-to-day operations from initiation to close-out according to regulatory guidelines. This role involves ensuring participant safety, adhering to approved protocols, handling administrative tasks, facilitating information flow, and coordinating study activities and personnel.
The Clinical Research Coordinator 2 assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. This role involves day-to-day operations of clinical research protocol implementation and study coordination duties from protocol initiation to study close-out.
Johns Hopkins University
The coordinator administratively manages clinical protocol implementation and ensures the logistical efficiency of study activities. Key duties include participant recruitment, consenting, data collection, and coordinating with the Institutional Review Board.
$17 - $30 / HOUR
22 days ago
Sanford Health
Organize and coordinate complex components of clinical trials, including patient recruitment, screening, and the administration of investigational treatments. Maintain accurate study documentation, resolve data queries, and collaborate with physician investigators to ensure protocol compliance.
$24 - $39 / HOUR
23 days ago
The coordinator will administratively manage clinical protocol implementation and ensure the logistical execution of study activities. Key duties include participant recruitment, consenting, data collection, and coordinating submissions to the Institutional Review Board.
1 month ago
The coordinator administratively manages clinical protocol implementation for neurology studies, ensuring adherence to protocols and validity of findings. Key duties include participant recruitment, consenting, data collection, and coordinating with the Institutional Review Board.
The coordinator administratively manages research protocol implementation and ensures efficient logistical execution of study activities. Key duties include data collection, record management, budget oversight, and coordinating study meetings.
Ann & Robert H. Lurie Children's Hospital of Chicago
The Clinical Research Coordinator assists investigators with the implementation and conduct of clinical research activities, including regulatory document maintenance and patient recruitment. They are also responsible for specimen collection, data entry into electronic capture systems, and monitoring study visits.
$46,280 - $75,670 / YEAR
The Clinical Research Coordinator will manage the daily operations of clinical trials, ensuring adherence to study protocols and safety regulations. They will serve as the primary liaison between the Principal Investigator, regulatory agencies, and study participants while handling recruitment, data collection, and documentation.
Valley Health System
Coordinate and implement clinical research protocols while providing direct nursing care to enrolled patients. Act as a patient advocate to ensure the safety, consistency, and accuracy of treatment regimens.
$48 - $60 / HOUR
The Clinical Research Coordinator will manage the logistical implementation of clinical protocols and ensure adherence to study activities. They will also provide administrative support for regulatory issues, including IRB submissions and participant recruitment.
The Senior Research Nurse coordinates and implements clinical trials within the oncology research program, ensuring protocol compliance and subject safety. They manage project documentation, oversee data collection, and provide education to patients and staff throughout the research process.
$75,100 - $131,700 / YEAR
University of Rochester
The role involves planning, coordinating, and implementing clinical research studies while ensuring adherence to regulatory guidelines and protocol standards. Responsibilities include managing participant enrollment, maintaining research records, and performing quality checks to ensure data accuracy and participant safety.
$25 - $35 / HOUR
Beth Israel Lahey Health
The Clinical Research Coordinator is responsible for recruiting and enrolling patients into clinical trials while ensuring strict adherence to study protocols. They also manage data extraction from medical records and assist with IRB correspondence and patient scheduling.
$22 - $31 / HOUR
The Geneva Foundation
The Physical Therapy Assistant will assist the Physical Therapist in patient instruction, including exercises and activities of daily living, and will be responsible for collecting, documenting, and reporting patient progress data. Responsibilities also include assisting in patient evaluations, making recommendations for mobility appliances, and ensuring compliance with research protocols and safety standards.
University Hospitals
The Clinical Research Nurse Specialist coordinates and implements clinical research studies in collaboration with the Principal Investigator. Responsibilities include recruiting participants, obtaining informed consent, maintaining regulatory documentation, and ensuring compliance with GCP guidelines.
2 months ago
The Clinical Research Coordinator 2 assists in the planning, implementation, and monitoring of clinical research studies, specifically focusing on genetic studies of Alzheimer's disease in African Ancestry communities. Responsibilities include participant recruitment, data collection, biological sample processing, and ensuring adherence to regulatory and protocol guidelines.
