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IRONWOOD PHYSICIANS,P.C.
Overview
Responsible for the timely submission and maintenance of accurate regulatory documents to pharmaceutical sponsors, IRBs, and contract research organizations. Oversees study initiation, monitoring, and closeout visits while ensuring compliance with federal regulations and international guidelines.
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Compensation
Salary not listed
Posted
15 days ago
Emory University
The coordinator will manage the recruitment, screening, and enrollment of participants for ophthalmic research studies while performing high-quality OCT imaging. Additionally, they will handle IRB submissions, extract retrospective data from EPIC, and segment images to support AI research.
17 days ago
The coordinator will recruit and enroll participants for ophthalmic research while performing high-quality OCT imaging. They are also responsible for maintaining IRB submissions, extracting data from EPIC, and segmenting images for AI research.
University Hospitals
Coordinate and implement clinical research studies in GI while providing safe, age-specific nursing care to participants. Manage regulatory documentation, recruit participants, and ensure compliance with GCP and sponsor guidelines.
24 days ago
City of Hope
Manage clinical trial patients by assessing eligibility, monitoring treatment responses, and ensuring strict adherence to IRB protocols. Coordinate care across multidisciplinary teams and educate patients and families on trial procedures and informed consent.
25 days ago
The Clinical Research Nurse coordinates oncology clinical trials, managing everything from patient recruitment and informed consent to data collection and biospecimen handling. They ensure strict adherence to federal regulations, study protocols, and institutional SOPs to protect human subjects.
29 days ago
Tufts Medicine
Assist the Principal Investigator in planning and implementing clinical research studies, including participant recruitment and screening. Manage study documentation, regulatory compliance, and data entry while ensuring adherence to IRB and FDA guidelines.
$47,924 - $59,895 / YEAR
1 month ago
Hoag
The Clinical Research Coordinator II manages all facets of clinical research trials, including planning, implementation, and closure, ensuring smooth and accurate processes in cooperation with physicians and sponsors. Responsibilities include protocol review, obtaining informed consent, managing study documentation, data collection, sample processing according to IATA standards, and adverse event reporting.
$37 - $57 / HOUR
Heluna Health
Coordinate and manage the implementation of biomedical intervention studies focusing on HIV and STI prevention. This includes managing study protocols, ensuring regulatory compliance, and overseeing data collection and laboratory issues.
$44 / HOUR
Manage clinical trial patients by assessing eligibility, monitoring treatment responses, and ensuring strict adherence to IRB protocols. Coordinate care across various settings while educating patients and families on trial procedures and informed consent.
CenExel
Coordinate all aspects of patient involvement in clinical trials while adhering to ICH, GCP, and company guidelines. Perform safety and efficacy assessments, document adverse events, and manage regulatory duties to ensure study compliance.
$26 - $27 / HOUR
The Clinical Research Coordinator II manages patient involvement and clinical trial activities while ensuring strict adherence to ICH, GCP, and protocol guidelines. They also assist with data reporting, safety assessments, and provide support to the Clinical Trial Manager in site operations.
Coordinate care for patients enrolled in clinical research trials by collaborating with physicians, pharmacists, and clinical research associates. Manage patient assessments, triage, and education while ensuring compliance with IRB protocols and FDA regulations.
Dartmouth-Hitchcock Health
The Clinical Research Nurse I provides care, education, and support to participants in less complex clinical research trials. Responsibilities include screening participants, administering investigational therapies, and ensuring adherence to research protocols and data security.
Coordinate care for patients enrolled in IRB clinical research trials by collaborating with physicians, pharmacists, and clinical research associates. Manage patient assessments, educate families on trial treatments, and ensure compliance with institutional and FDA regulations.
Mass General Brigham
The primary responsibility is conducting site monitoring visits to ensure human subject rights are protected and electronic case report forms are accurate and verifiable against source documents. This includes assessing protocol and regulatory compliance, reviewing site documentation, and maintaining communication with study staff regarding enrollment and data resolution.
$50,502 - $82,014 / YEAR
2 months ago
OneOncology
This role involves assisting with various clinical research activities under mentorship, including screening potential subjects for eligibility against trial criteria and managing informed consent records. The coordinator will also be responsible for procuring, processing, and shipping biospecimens according to protocol and regulations.
Shriners Children's
The Clinical Research Coordinator II independently oversees and ensures compliance of system-wide and local clinical research activities, acting as the primary liaison between participants, investigators, and sponsors. Key duties involve managing study operations according to GCP and regulatory guidelines, ensuring subject safety, and maintaining high-quality data collection and safeguarding.
3 months ago
The coordinator assists in managing all aspects of patient involvement in clinical trials from initiation to completion, ensuring strict adherence to ICH, GCP, protocol, and company guidelines. Key duties include organizing research information, observing subjects, scheduling data collection, documenting adverse events, and performing safety and efficacy assessments per protocol.
$29 - $33 / HOUR
4 months ago
The coordinator is independently responsible for managing all phases of multiple or complex clinical trials, ensuring strict adherence to ICH, GCP, protocol, and company guidelines. Key duties include coordinating patient involvement, organizing research information, monitoring study schedules, reporting adverse events, and managing research data quality.
$35 - $41 / HOUR
5 months ago
