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ALLIANCE CLINICAL LLC
Overview
The Assistant Clinical Research Coordinator supports the planning and execution of clinical trials by recruiting participants and collecting research data. They ensure all study activities comply with protocols, regulatory requirements, and institutional policies to maintain data integrity and participant safety.
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Compensation
$20 - $26 / HOUR
Posted
2 days ago
Always Best Care Senior Services - Knoxville, TN
Provide essential nonmedical in-home care for seniors, including assistance with activities of daily living and personal hygiene. Responsibilities also include meal preparation, medication reminders, and light housekeeping.
$15 - $17 / HOUR
Alliance For MultiSpecialty Research LLC
The Clinical Research Coordinator manages critical tasks for clinical studies, ensuring compliance with federal regulations and study protocols. Responsibilities include patient monitoring, data collection, phlebotomy, and coordinating with sponsors and IRBs.
Salary not listed
4 days ago
The Clinical Research Coordinator manages critical tasks for clinical studies, ensuring compliance with federal regulations, study protocols, and GCP guidelines. Responsibilities include patient monitoring, clinical data collection, phlebotomy, and coordinating with sponsors and IRBs.
12 days ago
MyMichigan Health
The Clinical Research Nurse provides direct patient care to study participants while ensuring strict adherence to research protocols and regulatory guidelines. They coordinate study activities, manage data collection, and maintain communication between sponsors, investigators, and participants.
16 days ago
The Clinical Research Nurse provides direct patient care to study participants while ensuring strict adherence to research protocols and regulatory guidelines. They coordinate study activities, manage data collection, and act as a liaison between investigators, sponsors, and participants.
23 days ago
The IMA Group
Coordinate clinical trials according to protocols and SOPs while maintaining accurate ALCOA documentation. Communicate with sponsors, CROs, and IRBs to ensure study data integrity and report adverse events.
$24 - $32 / HOUR
1 month ago
Coordinate clinical trials in accordance with study protocols and standard operating procedures while maintaining accurate documentation. Support investigators, communicate with regulatory bodies and sponsors, and ensure the integrity of study data and adverse event reporting.
$60,000 - $65,000 / YEAR
Maze Therapeutics
This role involves managing the day-to-day activities for Document Control and GxP Training programs, ensuring processes are completed accurately and on time through cross-functional collaboration. Key duties include managing the full document lifecycle, administering training within the LMS (ComplianceWire), and supporting broader quality system activities.
3 months ago
Summit Medical Group
The Advanced Practitioner will perform physical exams, order diagnostic tests, and develop treatment plans in a collaborative clinical environment. They are also responsible for educating patients and families while assisting physicians in managing acute and long-term medical needs.
