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Culmen International LLC
Overview
Assist physicians and scientists in developing and writing human and animal research protocols for military medicine programs. Coordinate regulatory submissions, manage study documentation, and facilitate the transition of projects from development to clinical operations.
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Compensation
Salary not listed
Posted
4 days ago
Coordinate research activities for IRB and IACUC-approved protocols, ensuring compliance with federal regulations and institutional policies. Support Principal Investigators by managing patient recruitment, specimen collection, and the maintenance of detailed regulatory documentation.
Oregon Health & Science University
The role involves coordinating recruitment, screening, and scheduling for clinical trials while managing patient data and regulatory compliance. Additionally, the assistant handles community outreach and social networking to increase participant diversity in women's health studies.
MPF Federal
The coordinator manages patient recruitment, consent, and study visits while ensuring strict adherence to clinical protocols and regulatory standards. They are responsible for data management, IRB submissions, and coordinating research activities in various environments, including naval ships.
$68,000 - $73,000 / YEAR
Johns Hopkins University
The specialist manages regulatory maintenance for oncology clinical trials, including IRB submissions and internal quality control. They also support program operations, train research staff, and facilitate compliance with institutional and federal research guidelines.
$48,000 - $84,100 / YEAR
1 month ago
American Addiction Centers
The Clinical Research Nurse II manages protocol-driven nursing care for trauma and burn patients, including subject recruitment, enrollment, and adherence to study protocols. They also coordinate with the research team and physicians to ensure high-quality data collection and compliance with regulatory guidelines.
$38 - $57 / HOUR
2 months ago
