Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
Mass General BrighamNew
Overview
The coordinator provides assistance on clinical research studies by recruiting and consenting patients, collecting data, and performing clinical tests. They are also responsible for maintaining study records in accordance with IRB rules and managing administrative compliance tasks.
Quick view →
Compensation
$21 - $29 / HOUR
Posted
New
Mass General Brigham
The coordinator assists with clinical research studies by recruiting and consenting patients, collecting data, and performing clinical tests. They are also responsible for scheduling protocol-mandated tests and ensuring compliance with regulatory requirements.
$29 / HOUR
2 days ago
Provides assistance on clinical research studies by collecting patient data, recruiting participants, and maintaining study records. Supports regulatory submissions, performs phlebotomy, and assists with data analysis and audits.
$22 - $29 / HOUR
Provides assistance on clinical research studies by recruiting and consenting patients, collecting data, and performing clinical tests. Responsibilities also include maintaining study documentation, updating data, and ensuring compliance with sponsor guidelines.
3 days ago
The coordinator will recruit and consent patients, collect and organize study data, and perform clinical tests like phlebotomy and EKGs. Additionally, they will operate MRI machines, administer psychological interviews, and manage regulatory documentation for the Neuroendocrine Unit.
The coordinator assists with clinical research studies by recruiting and consenting patients, collecting data, and performing clinical tests like phlebotomy and EKGs. They are also responsible for maintaining study documentation, ensuring regulatory compliance, and assisting with grant or journal submissions.
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.
$20 - $29 / HOUR
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
7 days ago
OneOncology
The Clinical Research Coordinator manages day-to-day oncology clinical trial operations from start-up to close-out. This includes conducting study visits, managing patient enrollment, and ensuring strict adherence to regulatory and protocol requirements.
Salary not listed
8 days ago
University of Miami
The coordinator manages entry-level clinical research activities, including participant screening, data collection, and protocol implementation. They are responsible for maintaining regulatory binders and ensuring compliance with international and local regulatory bodies.
The Clinical Research Coordinator manages day-to-day oncology clinical trial operations from start-up to close-out. This includes conducting study visits, managing patient enrollment, and ensuring regulatory compliance with ICH-GCP standards.
The coordinator manages entry-level clinical research tasks, including participant screening, data collection, and the implementation of simple research protocols. They are responsible for maintaining regulatory binders, monitoring study progress, and ensuring compliance with local and international guidelines.
The coordinator manages entry-level clinical research activities, including participant screening, data collection, and protocol implementation. They are responsible for maintaining regulatory binders, monitoring study progress, and ensuring compliance with local and international guidelines.
The Clinical Research Coordinator 2 manages the day-to-day operations of clinical research protocols from initiation to close-out. Key duties include participant recruitment, data collection, specimen processing, and ensuring adherence to regulatory and sponsor guidelines.
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.
Tufts Medicine
Assist the Principal Investigator in planning and implementing clinical research studies, including participant recruitment and follow-up. Manage regulatory documentation, perform basic laboratory activities, and ensure compliance with institutional and government human subject protections.
$44,779 - $55,978 / YEAR
9 days ago
Perelman School of Medicine at the University of Pennsylvania
Implement and coordinate clinical research activities within the Cardiovascular Division, specifically focusing on interventional and vascular cardiology studies. Responsibilities include screening and enrolling patients, performing phlebotomy, managing regulatory files, and ensuring protocol adherence.
$53,418 - $73,825 / YEAR
10 days ago
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.
