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UTHealth HoustonNew
Overview
Assists with the conduct and management of human subject research projects, including participant recruitment and data collection. Responsible for maintaining databases, preparing progress reports, and supporting grant proposals and regulatory submissions.
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Compensation
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Posted
New
UT Southwestern Medical CenterNew
The role involves performing technical research on genetic programs in the brain and analyzing mouse models of autism using molecular and genomic approaches. Additionally, the assistant is responsible for mouse colony management and general laboratory maintenance.
UT Southwestern Medical Center
The role involves performing technical research on genetic programs in the brain using molecular, biochemical, and genomic approaches. Responsibilities also include managing mouse colonies, general lab maintenance, and collaborating on scientific papers.
2 days ago
Mass General Brigham
The coordinator assists with clinical research studies by recruiting, evaluating, and consenting patients while collecting and organizing study data. They are also responsible for performing clinical tests like phlebotomy and EKGs and maintaining regulatory documentation.
$20 - $29 / HOUR
The Research Coordinator assists with clinical research studies by recruiting and consenting patients, collecting data, and performing clinical tests like phlebotomy and EKGs. They also ensure study compliance, maintain regulatory binders, and prepare data for analysis.
Prepares sterile and non-sterile products in adherence to USP and hospital policies while managing investigational prescriptions via the CTP system. Responsible for inventory management, temperature monitoring, and coordinating with study teams and sponsors for clinical trials.
$21 - $30 / HOUR
Provide technical assistance in medical and scientific research, focusing on mouse colony management and molecular techniques. Responsibilities include performing in vivo experiments, processing tissues, and collaborating on scientific papers.
Provide technical assistance in medical and scientific research, focusing on mouse colony management and molecular techniques. Responsibilities include performing in vivo experiments, processing tissues, and collaborating on scientific papers for publication.
UTHealth Houston
Coordinate day-to-day operations for clinical research studies, including participant recruitment, enrollment, and data management. Assist with regulatory submissions, budget preparation, and the creation of research papers and reports.
4 days ago
Avera Health
Coordinates and implements research study protocols, including participant recruitment, screening, and data collection. Manages laboratory specimens and ensures compliance with FDA regulations and Good Clinical Practices.
$22 - $37 / HOUR
$29 / HOUR
7 days ago
TriHealth
Acts as a liaison between study sponsors, investigators, and the IRB to coordinate and conduct clinical research studies. Responsible for enrolling subjects, collecting data, and ensuring all research activities comply with IRB and FDA standards.
Nevada System of Higher Education
The Research Assistant will recruit and enroll patients for clinical trials while ensuring adherence to all local, state, and federal research regulations. Responsibilities also include maintaining accurate study documentation, processing lab specimens, and assisting with IRB submissions and on-site sponsor visits.
$19 - $27 / HOUR
8 days ago
Froedtert
The RN performs primary nursing functions of assessing, planning, directing, and evaluating patient care in the emergency department. They collaborate with clinical and front office staff to ensure effective patient care is delivered to achieve optimal outcomes.
Cleveland Clinic
The Research Nurse Coordinator oversees the implementation and conduct of human subject research projects while ensuring adherence to protocols. They perform nursing assessments, manage regulatory documentation, and serve as a liaison between the research team and study participants.
Headlands Research
Coordinate all aspects of assigned clinical trials from site initiation through close-out while ensuring patient safety and data quality. Maintain strict compliance with protocols, FDA regulations, and GCP/ICH guidelines through accurate documentation and reporting.
$72,000 - $85,000 / YEAR
9 days ago
The Ohio State University
Coordinate and oversee clinical research protocols for hematology malignancies, focusing primarily on observational studies. Responsibilities include managing patient eligibility, obtaining informed consent, ensuring data integrity, and maintaining compliance with IRB and FDA regulations.
14 days ago
Perform complex laboratory procedures including frozen sections, paraffin preparation, and various specialized stains. Assist in laboratory management, quality control monitoring, and the instruction of medical students and new staff.
15 days ago
Perform complex laboratory procedures including frozen sections, paraffin sectioning, and various specialized stains for patient tissue. Assist in laboratory management, quality control monitoring, and the instruction of medical students and new staff.
Provide excellent patient care in a collegial and collaborative environment. Support the mission of patient care, innovation, medical research, and education within the health network.
