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Iterative Health
Overview
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.
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Compensation
Salary not listed
Posted
2 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.
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
Mid-Atlantic Permanente Medical Group PC
The Clinical Research Nurse coordinates the clinical trial study process, including patient recruitment, informed consent, and protocol-required assessments. They also ensure regulatory compliance by preparing IRB submissions and maintaining accurate study documentation throughout the lifecycle.
$79,370 - $99,213 / YEAR
University of Miami
The Clinical Research Nurse 1 ensures the integrity and quality of clinical research studies by conducting them in accordance with federal and institutional regulations. They also play a key role in participant recruitment, data collection, and patient education throughout the study process.
11 days ago
Florida Cancer Specialists
The Clinical Oncology Pharmacist will ensure the delivery of therapeutic medication monitoring, protocol management, medication information, education, and performance improvement to ensure safe, effective, and cost-efficient medication therapy. This role involves collaborating with Hematology/Oncology physicians and nursing staff to coordinate the drug therapy process for the patient population, including drug selection, dosing, and monitoring.
Washington University in St. Louis
Coordinate clinical research studies focusing on Epilepsy and rare pediatric diseases, acting as a liaison between investigators, sponsoring agencies, and participants. Manage all phases of study protocols, including participant recruitment, enrollment, and regulatory compliance reporting.
$47,400 - $71,200 / YEAR
1 month ago
University of Rochester
Coordinates administrative and operational activities for human subject research, including participant recruitment, screening, and protocol adherence. Acts as a liaison between the Principal Investigator, sponsors, and the Institutional Review Board to ensure regulatory compliance and data accuracy.
$21 - $30 / HOUR
Coordinates administrative activities for multi-site clinical research studies, including participant recruitment and consent. Manages study visits, ensures regulatory compliance, and assists in disseminating research findings through publications.
UCSF
The Clinical Research Coordinator manages and coordinates research protocols for pediatric diabetes studies, including participant recruitment and data collection. They oversee regulatory compliance, maintain study documentation, and facilitate communication between clinical staff, families, and investigators.
Sonic Healthcare USA
The Clinical Research Coordinator is responsible for recruiting and consenting study subjects for clinical trials while acting as a liaison between participants and the principal investigator. They also manage the operational aspects of bio-specimen procurement, including tracking recruitment metrics and coordinating blood collection handling.
The Clinical Research Coordinator manages and coordinates research protocols, ensuring data integrity and regulatory compliance across clinical studies. They act as an intermediary between departments, oversee study results, and assist with staff training and protocol oversight.
$38 / HOUR
University of California, Irvine
The Clinical Research Coordinator will manage clinical trial data and support research operations in compliance with Good Clinical Practices and internal policies. Responsibilities include patient recruitment, screening, consenting, and preparing regulatory submissions for the IRB and other committees.
Highmark Health
The Clinical Research Coordinator manages the initiation and completion of clinical trials while ensuring compliance with regulatory standards and patient safety. They interface with clinical staff and patients to provide education, obtain informed consent, and maintain accurate clinical data.
Hawthorne Health
Assist the Principal Investigator in overseeing clinical trials while ensuring adherence to study protocols and regulatory requirements. Provide medical oversight for study participants and maintain accurate documentation of all study-related data.
$150 / HOUR
Assist the Principal Investigator in managing clinical trials while ensuring adherence to study protocols and regulatory requirements. Provide medical oversight for study participants and maintain accurate documentation of all clinical trial data.
OneOncology
The Clinical Research Pharmacist oversees the pharmacy components of clinical trials, ensuring regulatory compliance and quality control for investigational products. They provide clinical support, patient education, and supervision to pharmacy staff while coordinating between research and pharmacy departments.
Mass General Brigham
The Research Nurse Coordinator is responsible for screening and enrolling patients in clinical trials while providing expert nursing care and symptom management. They collaborate with a multidisciplinary team to ensure protocol adherence and meticulous documentation of patient encounters.
$42 - $106 / HOUR
The Clinical Research Coordinator II manages complex clinical research activities, ensuring regulatory compliance and data integrity under the direction of the Principal Investigator. Responsibilities include coordinating study protocols, analyzing clinical data, and assisting in the preparation of manuscripts and grant proposals.
$52,600 - $78,900 / YEAR
Metro Infectious Disease Consultants
The Clinical Research Assistant provides non-clinical support for clinical trials, including data entry, equipment maintenance, and specimen management. They also assist Clinical Research Associates with monitoring tasks and ensure compliance with study protocols.
$50,000 - $53,000 / YEAR
