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Bausch+Lomb Companies Inc.
Overview
The Senior Principal Research Optometrist will design and lead clinical studies to support the development and launch of innovative eye care products. This role involves applying clinical and research expertise to study design, data analysis, and collaboration across functions.
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Compensation
$130,000 - $200,000 / YEAR
Posted
9 days ago
University of Texas Medical Branch (UTMB)
The coordinator obtains human subject data according to study protocols and manages general administrative duties to support clinical research. Key tasks include recruiting participants, maintaining regulatory documentation, and processing laboratory specimens.
Salary not listed
15 days ago
Care Access
The Clinical Research Coordinator II is responsible for screening, enrolling, and monitoring study subjects while ensuring strict adherence to protocol and regulatory compliance. They also manage patient coordination, perform clinical procedures, and maintain accurate study documentation.
$60,000 - $90,000 / YEAR
20 days ago
University of Massachusetts Medical School
The Research Nurse Coordinator is responsible for conducting complex protocols related to investigational drugs and devices, acting as a liaison between various stakeholders to ensure compliance with good clinical practice standards. They perform tasks such as patient screening, documentation of study events, and regulatory paperwork management throughout the study lifecycle.
The Research Nurse Coordinator is responsible for carrying out delegated tasks related to complex protocols testing investigational drugs and devices. They act as a liaison between various stakeholders to ensure good clinical practice standards throughout the study lifecycle.
$34 - $53 / HOUR
21 days ago
MyMichigan Health
The Clinical Research Nurse provides direct patient care to study participants while ensuring strict adherence to research protocols and regulatory guidelines. They coordinate study activities, manage data collection, and act as a liaison between investigators, sponsors, and participants.
Providence
Coordinates and maintains diverse activities for neurology clinical research trials, ensuring protocol adherence and timely study completion. Acts as a liaison for regulatory documents and manages subject recruitment, informed consent, and study documentation.
$32 - $49 / HOUR
22 days ago
Baptist Health South Florida
The Research Nurse is responsible for enlisting patients into clinical trials and ensuring strict adherence to study protocols and regulatory standards. They collaborate with physicians to determine patient eligibility and provide essential education to both staff and patients.
$73,861 - $98,235 / YEAR
26 days ago
UCSF
The coordinator will act as the primary recruiter, screening and enrolling participants for a phase 1 HIV prevention clinical trial. Responsibilities include managing study visits, data integrity, IRB requests, and coordinating staff and interns.
$38 / HOUR
29 days ago
Beth Israel Lahey Health
The Clinical Research Coordinator II is responsible for coordinating and administering multiple research studies, ensuring adherence to protocols and regulatory requirements. This role involves working closely with principal investigators and research staff, as well as interacting with study participants diagnosed with cardiovascular disease.
$19 - $31 / HOUR
1 month ago
Johns Hopkins University
The coordinator administratively manages clinical protocol implementation, ensuring adherence to study guidelines and validity of findings. Responsibilities include participant recruitment, consenting, data collection, and the processing and tracking of biospecimens.
$17 - $30 / HOUR
Cincinnati Eye Institute
The Clinical Research Coordinator oversees study protocols, ensures regulatory compliance, and manages site activities including patient recruitment and data documentation. They also coordinate with sponsors, manage study budgets, and perform study-specific testing and exams according to protocol guidelines.
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-down. Ensure compliance with regulatory requirements, informed consent, and safety reporting through remote and on-site monitoring.
Manage research activities at clinical sites, including site identification, start-up, and close-down processes. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
The Clinical Research Coordinator manages and executes clinical research protocols for breast oncology trials, overseeing administrative tasks, data integrity, and patient scheduling. They act as a liaison between sponsors and research staff while ensuring compliance with regulatory policies and assisting in patient care.
$40 - $45 / HOUR
University of Pennsylvania Perelman School of Medicine
The coordinator will assist with patient enrollment, follow-up, and the processing of biological specimens for the I3 biobank and related studies. Responsibilities include managing study documentation, maintaining databases, and coordinating regulatory submissions to the IRB.
$46,500 - $47,313 / YEAR
University of Pennsylvania
The coordinator will assist with patient enrollment, follow-up, and the procurement and processing of biological specimens for the I3 study. They are also responsible for maintaining study documentation, managing databases, and handling regulatory submissions to the IRB.
The US Oncology Network
The role involves screening and enrolling patients for cellular therapy trials and managing the informed consent process. Additionally, the nurse maintains regulatory documents and collaborates with physicians to ensure protocol compliance and patient safety.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Ensure compliance with informed consent, safety reporting, and regulatory requirements through remote and on-site monitoring.
Nationwide Children's Hospital
Assists with administrative components to ensure regulatory compliance for clinical research projects. Responsibilities include maintaining study binders, submitting IRB documents, and collecting investigator credentials.
