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Mid-Atlantic Permanente Medical Group PC
Overview
The Research Scientist II will design and implement major health services and epidemiology-related research projects in infectious diseases. They will also secure external funding and disseminate findings through publications and presentations.
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Compensation
$152,776 - $190,970 / YEAR
Posted
10 days ago
University of Massachusetts Medical School
The Clinical Research Coordinator I is responsible for coordinating regulatory activities and managing data collection for research protocols. This includes obtaining consent from participants, scheduling study visits, and ensuring compliance with protocols.
Salary not listed
23 days ago
The Clinical Research Coordinator I is responsible for coordinating regulatory activities and managing data collection for research protocols. This includes obtaining consent from participants, scheduling visits, and ensuring compliance with study protocols.
$40,000 - $48,000
Ann & Robert H. Lurie Children's Hospital of Chicago
The Research Coordinator II will manage research projects, including participant recruitment, data collection, and quality assurance. They will also coordinate with clinical partners and community organizations to ensure adherence to study protocols.
$49,920 - $81,619 / YEAR
1 month ago
NYU Langone Health
The Research Coordinator will manage day-to-day research activities, including study design, data collection, and regulatory submissions to the IRB. They will also coordinate participant recruitment and support the development of manuscripts and abstracts for dissemination.
$66,300 - $66,300 / YEAR
University of Colorado
The Clinical Research Coordinator oversees day-to-day operations of clinical trials, including patient recruitment and the informed consent process. They also ensure regulatory compliance with FDA guidelines and perform clinical tasks such as blood sample collection and processing.
$49,899 - $78,665 / YEAR
Norwalk Hospital Association
The Clinical Research Coordinator collaborates with departmental leadership and research staff to coordinate all aspects of clinical research studies, including patient screening, recruitment, and protocol implementation. They are responsible for maintaining communication with various stakeholders and ensuring compliance with regulatory requirements.
$30 - $56 / HOUR
2 months ago
This role involves supporting clinical research labs by assisting with and overseeing the day-to-day operations of clinical trials and studies. Key duties include managing subject eligibility, performing the informed consent process, collecting and processing patient specimens, and accurately collecting and analyzing research data.
$48,446 - $61,623 / YEAR
This role involves supporting clinical research labs by assisting with and overseeing the day-to-day operations of clinical trials and studies. Key duties include obtaining subject medical history, confirming eligibility, performing the informed consent process, collecting and processing specimens, and accurately analyzing research data.
University of Chicago
This role provides technical research support for basic clinical studies, focusing on collecting, documenting, and reporting data, alongside managing administrative and operational tasks for clinical research activities across the University. Key duties include collecting biometric data and biospecimens, interacting with patients regarding study participation, performing phlebotomy, processing samples, and ensuring strict adherence to GCP and regulatory guidelines.
$19 - $24 / HOUR
