- University of Maryland, Baltimore (Baltimore, MD)
- …of treatment fidelity measures. This individual will be responsible for executing the research project according to the approved IRB protocol, including holding ... will be needed Training will be provided for the Research Interventionist related to human subjects' ...may report concerns or questions to the Title IX Coordinator . Read the UMB Notice of Non-Discrimination for more… more
- Arkansas Children's (Little Rock, AR)
- …job description for details. **Time Type:** Full time **Department:** CC033005 Research Account Administration **Summary:** Set up clinical trial budgets and ... contracts for the clinical research program. Provide guidance and assistance to coordinators and...summarizing the clinical trial activities for the financial account review . Invoice for costs as directed by the sponsor… more
- University of Colorado (Aurora, CO)
- …be expected to complete human research subject's protection and other institutional review board training requirements; + Assist CCBD physicians with ... with or fluency in medical Spanish;_ + _Experience with clinical trials and clinical research , including human research subjects' and/or CITI training;_ +… more
- Binghamton University (Binghamton, NY)
- …and troubleshooting experimental equipment + Writing and managing experimental protocols with the Institutional Review Board + There will also be ... will participate in, undertake and assist with faculty-sponsored cognitive neuroscience research involving human subjects and magnetic resonance imaging (MRI).… more
- University of Colorado (Aurora, CO)
- …and institutional policies + Contribute to regulatory submissions, including IRB applications and protocol amendments related to pharmacy operations + Conduct a ... **Preferred Qualifications:** + Experience with investigational drug services, clinical research operations, or IRB /regulatory processes + Research… more
- University of Colorado (Aurora, CO)
- … IRB applications. + Support grant proposals, including drafting human subjects sections, recruitment plans, budgets, and Just-in-Time documentation. + Scientific ... to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator at ###@cuanschutz.edu (https://apptrkr.com/get\_redirect.php?id=6663891&targetURL=###@cuanschutz.edu)… more
- University of Utah (Salt Lake City, UT)
- …Schedule Summary** **VP Area** President **Department** 01938 - HCI Mary Playdon Research Prog **Location** Campus **City** Salt Lake City, UT **Type of ... Posting **Pay Rate Range** 62232.00 **Close Date** 06/30/2026 **Priority Review Date (Note - Posting may close at any...Huntsman Cancer Institute, is seeking a highly motivated Postdoctoral Research Associate to join the lab of Dr. Mary… more
- Arkansas Children's (Little Rock, AR)
- …team of regulatory professionals and work closely with investigators, sponsors, and institutional review boards (IRBs) to facilitate regulatory submissions and ... **Recommended Work Experience:** **Required Certifications:** **Recommended Certifications:** Certified Clinical Research Coordinator (CCRC) - Association of Clinical… more
- University of Colorado (Aurora, CO)
- …data. + Screen and consent eligible patients for research studies under IRB -approved protocols. + Collect and process human biospecimens (eg, blood, pleural ... study databases. + Maintain accurate records in compliance with regulatory and institutional guidelines. + Assist with IRB submissions, amendments, and renewals.… more
- University of Colorado (Aurora, CO)
- …design and data collection, and familiarity with the processes to ensure ethical human subjects research . + Proficiency with Microsoft Office Applications - ... to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator at ###@cuanschutz.edu (https://apptrkr.com/get\_redirect.php?id=6623183&targetURL=###@cuanschutz.edu)… more