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Iterative Health
Overview
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.
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Compensation
Salary not listed
Posted
3 days ago
Avera Health
Coordinates and implements research study protocols, including participant recruitment, data collection, and laboratory specimen processing. Collaborates with investigators and healthcare providers to ensure safe, compliant research procedures for maternal and child health studies.
$21 - $37 / HOUR
4 days ago
Coordinates and implements research study protocols, including participant recruitment, screening, and data collection. Manages laboratory specimens and ensures compliance with FDA regulations and Good Clinical Practices.
$22 - $37 / HOUR
Clinilabs
The Polysomnographic Technologist prepares and collects data for research and clinical duties, ensuring the accuracy of recording procedures. Responsibilities also include direct contact with subjects for assessments and maintaining laboratory equipment.
$47 - $55 / HOUR
6 days ago
Evolution Research Group
The EMT/Paramedic assists in clinical trials by dispensing investigational drugs and collecting biological samples. They are responsible for performing ECGs, venipuncture, and ensuring all procedures follow Good Clinical Practices (GCP).
9 days ago
The Unit Clinician assists with clinical trial execution by performing procedures such as venipuncture, ECGs, and biological sample processing. They are responsible for dispensing investigational products and maintaining accurate documentation in subject charts according to protocol.
$39 - $45 / HOUR
The LPN or RN will assist in the conduct of clinical trials by dispensing investigational drugs and collecting biological samples. They are responsible for performing clinical procedures, maintaining accurate subject charts, and ensuring compliance with Good Clinical Practices.
Glaukos
The CRA is responsible for assessing, training, and monitoring clinical research sites to ensure data integrity and protocol compliance. This includes conducting site visits, managing investigator relationships, and overseeing the accountability of investigational products.
$73,600 - $85,000 / YEAR
10 days ago
The CRC II manages industry-sponsored clinical trials, overseeing patient recruitment, study visits, and the collection of clinical data. They are responsible for maintaining high-quality documentation and coordinating communication between sponsors, CROs, and the Principal Investigator.
15 days ago
University of California, Irvine
Coordinate and manage Phase I-IV cancer-related clinical trials, ensuring adherence to GCP, SOPs, and university policies. Act as a liaison between sponsors, regulatory agencies, and the research team while managing patient recruitment and data collection.
Care Access
The Clinical Research Coordinator I, RN conducts delegated clinical tasks and monitors research participants to ensure compliance with protocols and regulations. They are responsible for patient coordination, documentation, and recruitment activities.
21 days ago
Pinnacle Clinical Research
The Pharmacy Assistant supports day-to-day clinical trial operations, including receiving, documenting, and dispensing investigational products. They are also responsible for maintaining pharmacy logs, coordinating temperature calibrations, and providing patient education.
22 days ago
HUTCHINSON CLINIC P A INC
Coordinate clinical trial protocols including study initiation, recruitment, and regulatory compliance. Act as a liaison between providers, patients, and study representatives while managing medical documentation and patient visits.
23 days ago
University of Maryland Medical System
The role involves coordinating clinical research trials in radiation oncology, including protocol submission, patient recruitment, and data management. The coordinator acts as a liaison between sponsors, investigators, and review boards to ensure regulatory compliance and study integrity.
San Francisco AIDS Foundation
Perform high-volume phlebotomy and manage the processing and quality assurance of laboratory specimens. Additionally, serve as an HIV testing counselor providing education and prevention services to at-risk communities.
$34 - $37 / HOUR
Perform high-volume phlebotomy and manage the processing and transport of laboratory specimens. Conduct quality assurance on tests and serve as an HIV testing counselor to provide patient education.
NYU Langone Health
The Research Coordinator provides coordination for medical research studies, including patient recruitment, enrollment, and data collection. They also manage regulatory documents, assist with grant submissions, and ensure compliance with HIPAA and Good Clinical Practices.
$66,300 - $66,300 / YEAR
24 days ago
ALS
The coordinator plans and develops safety and efficacy research studies under the supervision of a Principal Investigator. They oversee day-to-day clinical activities, supervise research assistants, and manage study workflow and reporting.
25 days ago
Baptist Health South Florida
The Nurse Research Coordinator supports the Clinical Research staff by coordinating and administering clinical study protocols in cooperation with the Principal Investigator. This role includes ensuring compliance with regulatory requirements and maximizing subject participation in cardiovascular research protocols.
26 days ago
Tulane University
Coordinate day-to-day operations for cardiovascular disease studies, acting as a liaison between patients, investigators, and sponsors. Responsibilities include screening and enrolling patients, ensuring protocol compliance, and managing regulatory documentation.
27 days ago
