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ICON plc
Overview
The role involves conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. Additionally, the CRA will collaborate with site staff and perform data review to maintain high-quality clinical trial documentation.
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Compensation
Salary not listed
Posted
18 days ago
University of Tennessee
The Research Study Coordinator 2 plans and coordinates clinical research activities within the Department of Obstetrics & Gynecology. The role involves managing research protocols and regulatory guidelines to achieve project goals.
$4,182 - $5,000 / MONTH
22 days ago
Albert Einstein College of Medicine
The Study Coordinator manages asthma-related research projects by overseeing participant recruitment and ensuring data integrity. They serve as a liaison between stakeholders and handle regulatory documentation for the IRB and funding agencies.
$58,500 / YEAR
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.
26 days ago
Maine Eye Center
The coordinator assists the Principal Investigator in implementing clinical research studies, focusing on participant recruitment and eligibility screening. They are responsible for maintaining regulatory documentation, performing data entry, and ensuring compliance with FDA and IRB guidelines.
1 month ago
Mayo Clinic
The RN Study Coordinator is responsible for coordinating and delivering nursing care, including direct patient care and education in clinical and research settings. They manage all phases of the research process and ensure compliance with regulatory laws and institutional guidelines.
$30 - $52 / HOUR
Johnson & Johnson Innovative Medicine
The Clinical Trials Assistant supports the clinical study team with project communications, site payments, and file management. They are responsible for maintaining clinical databases, processing regulatory documents, and ensuring study supplies are managed effectively.
$41,000 - $66,700 / YEAR
The Research Study Coordinator manages investigator-initiated research activities, including regulatory paperwork and IRB applications. They are also responsible for maintaining study files and essential trial documents to ensure compliance.
$22 / HOUR
MESO SCALE DIAGNOSTICS, LLC.
The Senior Study Coordinator supports bioanalytical laboratory studies by drafting protocols, managing study documentation, and performing quality control reviews. They work closely with Principal Investigators to track project timelines, deliverables, and ensure compliance with GLP and GCLP standards.
$67,900 - $101,000 / YEAR
Medpace, Inc.
The Clinical Nurse Study Coordinator is responsible for the accurate administration of medications, monitoring of adverse events, and performing clinical procedures according to study protocols. They also collaborate with project managers and investigators to ensure operational flow and data integrity.
2 months ago
Ardelyx
The Clinical Research Associate II provides sponsor oversight of assigned investigative sites, focusing on high-quality protocol execution and compliance with GCP and regulatory requirements. This role involves monitoring site performance through data review, supporting all phases of the clinical trial lifecycle, and ensuring timely collection and maintenance of essential regulatory documents.
$99,000 - $121,000 / YEAR
BioAgilytix
The Study Coordinator will be responsible for maintaining accurate study records, tracking project samples, and supporting assay quality control testing performed during sample analysis. This role also involves supporting study start-up, end-of-study activities, and maintaining essential documentation like CoAs and reagent records.
NCIRE - The Northern California Institute for Research and Education, Inc.
The incumbent will serve as the Study Coordinator, providing day-to-day coordination for several research studies under the direction of the Multiple Principal Investigators. Responsibilities include maintaining documentation, overseeing progress tracking, recruiting participants, conducting informed consent, scheduling visits, data management, and assisting with progress reports.
$25 - $41 / HOUR
Ionis Pharmaceuticals, Inc.
This role serves as the primary liaison between Ionis, Contract Research Organizations (CROs), and internal teams, focusing on the smooth execution of nonclinical study conduct. Operational duties include facilitating study contracts, managing test article requests, coordinating sample logistics, and maintaining study documentation and tracking systems.
$40 - $52 / HOUR
3 months ago
