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Mass General Brigham
Overview
Manages cardiovascular clinical trials, including subject recruitment, enrollment, and the maintenance of regulatory documentation. Performs clinical tests such as phlebotomy and EKGs while managing research data and biological samples.
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Compensation
$20 - $29 / HOUR
Posted
2 days ago
The coordinator assists with clinical research studies by recruiting, evaluating, and consenting patients while collecting and organizing study data. They are also responsible for performing clinical tests like phlebotomy and EKGs and maintaining regulatory documentation.
Ann & Robert H. Lurie Children's Hospital of Chicago
This role coordinates and manages the initiation and regulatory compliance of clinical research studies, including preparing documents, managing study conduct across departments, and overseeing all aspects of clinical research visits. Responsibilities also include managing participant engagement, collecting specimens, recording data, assisting with financial aspects, and participating in investigator meetings.
$49,920 - $81,619 / YEAR
6 days ago
$29 / HOUR
7 days ago
University of Miami
The coordinator manages simple clinical research protocols, including participant pre-screening, enrollment, and data collection. They are also responsible for monitoring adverse events, ensuring regulatory compliance, and maintaining study-specific regulatory binders.
Salary not listed
Nira Medical
Perform clinical duties including vital signs, blood draws, and ECGs while managing laboratory specimens. Responsible for accurate data entry into EDC systems and ensuring compliance with GCP, IRB, and HIPAA regulations.
9 days ago
Headlands Research
Support clinical trials by preparing study documents, recruiting participants, and conducting patient-facing procedures like vital signs and phlebotomy. Manage study data entry in EDC and CTMS systems while ensuring compliance with FDA and GCP guidelines.
$22 - $27 / HOUR
Provides assistance on clinical research studies by recruiting and consenting patients and collecting study data. Performs clinical tests such as phlebotomy and EKGs while maintaining regulatory binders and documentation.
$21 - $29 / HOUR
16 days ago
The Clinical Research Coordinator assists with clinical research studies by recruiting and consenting patients, collecting data, and performing clinical tests. They also maintain study documentation, prepare data for analysis, and ensure compliance with regulatory protocols.
Nova Medical Services
The Clinical Research Coordinator manages the planning and execution of clinical trials, ensuring strict adherence to ICH, GCP, and regulatory guidelines. Key duties include coordinating patient visits, maintaining regulatory documentation, and managing study data entry and verification.
$23 - $25 / HOUR
17 days ago
SerenaGroup Inc
The Clinical Research Coordinator manages day-to-day clinical trial activities, including patient recruitment, screening, and study visit execution. They are responsible for maintaining accurate study documentation and ensuring compliance with FDA and ICH-GCP guidelines.
20 days ago
The coordinator supports clinical research studies on neuromuscular diseases by recruiting and consenting patients and performing clinical tests. They are also responsible for maintaining research data, performing QA/QC checks, and assisting the PI with reports and presentations.
$24 - $39 / HOUR
23 days ago
The coordinator supports the GROWTH study by managing regulatory documents, recruiting eligible subjects, and collecting and processing specimens. They are also responsible for data entry into electronic platforms and coordinating study visits and reimbursements.
$46,280 - $75,670 / YEAR
24 days ago
The coordinator supports clinical trials for rare genetic disorders by managing regulatory documents and recruiting eligible study subjects. They are also responsible for collecting specimens, entering data into electronic platforms, and coordinating study visits.
$22 - $36 / HOUR
27 days ago
Coordinates clinical research studies by recruiting and consenting patients, collecting data, and performing clinical tests. Responsible for maintaining regulatory binders, performing data analysis, and assisting the Principal Investigator with reports and presentations.
28 days ago
Genesis Orthopedics & Sports Medicine
Coordinate and manage clinical trials from startup to closeout, including participant recruitment, screening, and visit conduction. Maintain accurate study data, regulatory binders, and ensure strict adherence to GCP and protocol requirements.
Tufts Medicine
Assist the Principal Investigator in planning and implementing clinical research studies, including participant recruitment and screening. Manage study documentation, regulatory compliance, and data entry while ensuring adherence to IRB and FDA guidelines.
$47,924 - $59,895 / YEAR
29 days ago
Lurie Children's Hospital
The coordinator manages the GROWTH study by handling regulatory documents, recruiting subjects, and collecting/processing specimens. They are also responsible for data entry into electronic platforms and coordinating study visits and reimbursements.
The Clinical Research Coordinator assists in planning and implementing cardiovascular clinical research studies, including participant recruitment, screening, and data collection. They are responsible for maintaining regulatory compliance, managing study documentation, and ensuring patient safety throughout the research process.
This role involves assisting the Principal Investigator in planning and implementing clinical research studies, including participant recruitment, screening, and follow-up activities. Responsibilities also cover maintaining regulatory compliance, managing study documentation, performing basic lab activities, and coordinating data collection and query resolution.
