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Mass General BrighamNew
Overview
Coordinate and run study visits involving neuroimaging and biological sample collection for infection-associated health conditions. Manage IRB compliance documents, screen potential participants, and assist with data processing and analysis.
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Compensation
$21 - $29 / HOUR
Posted
New
Arizona Liver Health
Coordinate clinical research trials by recruiting participants, performing clinical procedures like phlebotomy and vitals, and managing study data. Ensure strict adherence to regulatory guidelines, maintain study documentation, and collaborate with sponsors and internal staff.
$28 - $36 / HOUR
2 days ago
Mass General Brigham
Coordinate NIH-funded studies on substance use disorder by managing participants, data, and IRB correspondence. Perform clinical tests such as phlebotomy and EKGs while maintaining study documentation and regulatory binders.
$29 / HOUR
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.
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.
$20 - $29 / HOUR
The Research Coordinator assists with clinical research studies by recruiting and consenting patients, collecting data, and performing clinical tests like phlebotomy and EKGs. They also ensure study compliance, maintain regulatory binders, and prepare data for analysis.
Iterative Health
The Clinical Research Coordinator manages daily clinical trial activities, including patient recruitment, protocol adherence, and clinical procedures like blood draws and IV administration. They also ensure data integrity, maintain study documentation, and act as the primary point of contact for study participants.
Salary not listed
3 days ago
The Clinical Research Coordinator I supports and coordinates daily clinical trial activities, including administratively and clinically managing industry-sponsored trials, problem-solving, and ensuring protocol adherence. Key duties involve leading patient recruitment, scheduling visits, conducting procedures like blood draws and injections, and dispensing study medication.
Duke Careers
The Associate in Research will assist with IRB protocols, recruit and consent study participants, and perform EEG recordings and neuromodulation. They are also responsible for data compilation, report preparation, and maintaining lab records.
Seattle Children's
Support the Community Engagement Core and the Pediatric Pain and Sleep Innovations lab by facilitating research activities. Responsibilities include participant recruitment, administering assessments, and managing data collection and tracking.
$35 - $53 / HOUR
Mohawk Valley Health System
The Clinical Research Nurse facilitates and coordinates daily clinical trial activities, ensuring adherence to protocols and regulatory requirements. They work closely with the Principal Investigator to manage study documentation, participant recruitment, and data collection.
$75,000 - $115,000 / YEAR
4 days ago
Ascension
Coordinate administrative and clinical aspects of multiple oncology research projects, including participant recruitment and monitoring. Collaborate with investigators and sponsors to ensure protocol compliance and manage IRB documentation and audits.
Headlands Research
The Nurse Practitioner or Physician Assistant will serve as a Sub-Investigator, ensuring the safety and welfare of clinical trial subjects. Responsibilities include conducting medical history interviews, performing physical examinations, and reviewing lab results according to research protocols.
7 days ago
Nemours Children's Health
The primary function is to recruit volunteers for the Lung Health Cohort study by building relationships with community organizations and members through various outreach activities. Duties include attending community meetings, networking, distributing information, and maintaining participant records in compliance with funding requirements.
Vanderbilt University Medical Center
Coordinate clinical trial protocols, patient consent processes, and the preparation of IRB and regulatory documents. Identify and recruit research subjects while managing data collection and lab specimen shipping.
Vail Health Hospital
The Clinical Research Coordinator manages clinical trials by ensuring patient safety, regulatory compliance, and accurate data collection. They coordinate patient recruitment, maintain study documentation, and facilitate communication between investigators, sponsors, and clinical staff.
$32 - $44 / HOUR
8 days ago
Nevada System of Higher Education
The Research Coordinator will recruit and screen clinical trial participants, manage regulatory documentation, and provide clinical care services including patient monitoring and sample processing. They will also assist with study budget proposals, data entry, and ensure adherence to institutional and federal protocols.
$25 - $37 / HOUR
Mercyhealth Wisconsin and Illinois
The Clinical Research Coordinator is responsible for recruiting and consenting study participants, managing regulatory documentation, and ensuring protocol adherence. They also handle specimen collection and processing while maintaining accurate data submission and reporting adverse events.
$27 - $42 / HOUR
9 days ago
Systimmune
The Senior CRA manages and oversees assigned clinical study sites to guarantee data quality and patient safety, adhering to ICH-GCP guidelines, local regulations, and SOPs. Responsibilities include performing all types of monitoring visits, managing site compliance, assisting in study plan development, and overseeing recruitment strategies.
$90,000 - $130,000 / YEAR
