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University of Massachusetts Medical School
Overview
The Clinical Research Coordinator I is responsible for coordinating regulatory activities and managing data collection for research protocols. This includes obtaining consent from participants, scheduling study visits, and ensuring compliance with protocols.
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Compensation
Salary not listed
Posted
23 days ago
Washington University in St. Louis
The Clinical Research Coordinator manages complex clinical research studies, ensuring protocol compliance and acting as a liaison between investigators, sponsors, and participants. They are responsible for data collection, adverse event reporting, and the preparation of research reports and publications.
$52,600 - $78,900 / YEAR
The Clinical Research Coordinator I is responsible for coordinating regulatory activities and managing data collection for research protocols. This includes obtaining consent from participants, scheduling visits, and ensuring compliance with study protocols.
$40,000 - $48,000
United Urology Group
The Research Coordinator will screen, enroll, and follow study subjects for clinical trials, ensuring protocol compliance and monitoring. Responsibilities include conducting clinical trials, enrolling subjects, and managing follow-up procedures.
$27 - $31 / HOUR
24 days ago
Valley Health System
The Research Fellow will participate in advanced cardiovascular research, contributing to ongoing studies and developing independent projects. Responsibilities include study design, data analysis, manuscript preparation, and professional presentation of findings.
$80,340 / YEAR
25 days ago
St. Joseph Hospital & Medical Center
The Clinical Research Specialist leads and manages complex clinical research studies while ensuring protocol adherence and scientific integrity. They oversee data collection, regulatory compliance, and act as a liaison between sponsors, investigators, and study subjects.
$24 - $36 / HOUR
1 month ago
CTI Clinical Trial and Consulting Services
The Study Designer translates customer expectations into laboratory services and provides comprehensive protocol reviews. They manage technical changes, ensure SOP compliance, and collaborate with internal departments to meet client needs.
The coordinator manages all phases of clinical research study protocols to ensure regulatory compliance and participant safety. They also assist investigators with data interpretation, manuscript preparation, and the development of research project plans.
UCSF
Provide expert toxicology information to healthcare professionals and the public regarding the diagnosis and treatment of poisoning. Manage high-volume hotline calls while utilizing computerized information systems to ensure accurate clinical assessments.
2 months ago
Johns Hopkins University
The Sr. Research Project Coordinator oversees the daily operations of complex research projects, making independent decisions that affect research conduct, and assists senior staff in ensuring the operational feasibility of proposed study designs. This role involves developing standard operating procedures, overseeing data collection tools, ensuring regulatory compliance, and contributing to budget formulation and data system management.
$41,300 - $72,300 / YEAR
4 months ago
