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University of Miami
Overview
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.
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Compensation
Salary not listed
Posted
11 days ago
Sago
The Research Project Interviewer supports study execution by conducting subject interviews, obtaining informed consent, and managing study visits. They also ensure all documentation complies with regulatory requirements and collaborate with the clinical project management team.
$15 / HOUR
1 month ago
Trinity Health
The In-Home Attendant provides essential care services to maintain the independence of participants by assisting with activities of daily living, physical activity, and general support tasks. This role also involves monitoring participant safety, identifying changes in physical or emotional status, and ensuring compliance with safety and infection control standards.
CenExel
The coordinator ensures the highest standards of data quality and participant safety are maintained, along with adherence to protocols, SOPs, and regulatory guidelines. This involves assisting the QA Manager, reviewing various study documents for trends, and performing ongoing quality reviews of study records and documentation.
2 months ago
Syneos Health
The Research Nurse I will provide front-line medical support for study participants, ensuring their safety and comfort, and acting swiftly in adverse event situations. Key duties include performing clinical procedures like IV insertions and venipuncture, monitoring participants, and guiding them through the informed consent process.
$62,000 - $108,600 / YEAR
University of Rochester
The specialist will oversee the screening, assessment, and retention of participants in a Randomized Controlled Trial (RCT) involving Deaf adults with mental health disorders, conducting all study activities remotely via Zoom. Key duties include performing mental health and suicide risk assessments in ASL, coordinating follow-up assessments, assisting with data management, and ensuring participant safety according to protocol.
$21 - $30 / HOUR
This role involves assisting in the planning, coordination, implementation, monitoring, and evaluation of assigned clinical research studies, ensuring adherence to regulatory guidelines from initiation to close-out. Key functions include coordinating participant enrollment, managing study documentation, performing data entry and quality checks, and maintaining study continuity for moderate-sized studies.
$25 - $35 / HOUR
3 months ago
LIFE Pittsburgh
The Community Care Nurse promotes and maintains participant health during peak weekend hours by conducting in-person clinical assessments, post-hospital discharge follow-up, and urgent illness evaluations within an Interdisciplinary Team setting. This role collaborates with the Weekend On-Call RN to support triage, ensure timely field response, and enhance weekend clinical responsiveness to reduce unnecessary emergency department utilization.
The Certified Nurse Assistant provides necessary care services to meet the personal needs, support, and health status of participants both in clinic and at home, focusing on maintaining independence in daily living activities. Responsibilities include participating in ongoing participant assessment, reporting on care provided, assisting with physical activity, and ensuring participant safety by identifying hazards and emergency situations.
Rockefeller University
The Study Research Coordinator focuses on trial operations and participants, coordinating day-to-day activities and assisting investigators with preparing and submitting IRB applications. Duties include screening, enrolling, and monitoring participants while ensuring accurate data collection and safeguarding participant safety.
The coordinator ensures the highest standards of data quality and participant safety are maintained, along with adherence to protocols, SOPs, and regulatory guidelines. This involves assisting the QA Manager, reviewing various monitoring reports and logs for trends, and performing ongoing quality reviews of study documentation.
Temple University Health System
The Clinical Research Nurse will coordinate and facilitate clinical research protocols, ensuring participant recruitment, protocol compliance, and data quality. They will work closely with the clinical research team to develop tools for monitoring trial accrual and manage study activation and protocol amendments.
4 months ago
The coordinator ensures the highest standards of data quality and participant safety are maintained, adhering strictly to protocols, SOPs, and regulatory guidelines. Key duties involve assisting the QA Manager with program development, reviewing monitoring reports for trends, and performing ongoing quality reviews of study documentation.
$53,000 - $55,000 / YEAR
5 months ago
