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Emory University
Overview
Perform defined research and laboratory tests according to prescribed protocols and schedules. Maintain laboratory records, manage supplies, and compile data for publications and grants.
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Compensation
Salary not listed
Posted
14 days ago
The Clinical Research Coordinator II manages administrative activities for clinical trials, including database management and regulatory submissions. They are responsible for recruiting and consenting participants, ensuring protocol compliance, and supervising specimen collection.
The coordinator manages administrative activities for clinical trials, including data entry, patient recruitment, and specimen collection. They are also responsible for maintaining equipment, tracking regulatory submissions, and coordinating study procedures.
The coordinator manages administrative activities for clinical trials, including database management, participant recruitment, and consenting. They ensure protocol compliance, prepare regulatory submissions, and oversee the collection and processing of study specimens.
Perform routine animal care duties in a research setting, including feeding and maintaining sanitary conditions. Observe animal behavior and collect specimens while assisting with restraint and housing maintenance.
15 days ago
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.
The coordinator manages administrative activities for clinical trials, including database management, participant recruitment, and ensuring protocol compliance. They are also responsible for processing study specimens and preparing regulatory submissions.
The role involves developing biochemical and cell-based assays for high throughput screening of small molecule libraries. The scientist will also execute assays for structural optimization of hit compounds and collaborate with medicinal chemists.
21 days ago
Johns Hopkins University
The Research Technologist performs routine laboratory assays and experiments following established protocols. Responsibilities include collecting project data, maintaining lab equipment, and training users on standard equipment operation.
$16 - $26 / HOUR
22 days ago
The coordinator manages administrative activities for clinical trials, including data entry, patient recruitment, and specimen collection. They also coordinate study services, maintain regulatory submissions, and monitor charges for research projects.
25 days ago
The Clinical Research Coordinator II manages administrative activities for clinical trials, including database management and regulatory submissions. They are responsible for recruiting and consenting participants, supervising specimen collection, and ensuring strict protocol compliance.
Boston University
The role involves coordinating brain tissue requests, performing dissections, and conducting immunohistochemical analyses. Additionally, the specialist manages specimen-tracking databases and provides oversight and training to research assistants and interns.
$48,075 - $60,625 / YEAR
29 days ago
Perform and assist in research studies focusing on the molecular immune response to infections using animal models and molecular biology techniques. Manage basic laboratory organization and maintain mouse breeding colonies.
$17 - $22 / HOUR
1 month ago
Provides technical and operational support for a research program focused on mouse models. Responsibilities include performing molecular assays, maintaining transgenic colonies, and managing laboratory inventory.
$40,000 - $44,000 / YEAR
The coordinator manages administrative activities for clinical trials, including database management and regulatory submissions. They are responsible for recruiting and consenting participants, processing specimens, and ensuring strict protocol compliance.
