- ICON Clinical Research (Lenexa, KS)
- …ensures what we do, we do well. **What will you be doing?** Maintains study documents and utilizes company systems to manage the bioanalytical data in support of ... clinical/pre-clinical studies . Provides administrative support to project team members in...and maintains these documents for regulatory submissions. + Organizes study information and supplies. Maintains project timelines, ensure project… more
- New York University (New York, NY)
- The Research Associate (Part-Time) will support a study titled Which Studies Shape the Narrative? Analyzing How Education Research Reaches Policy Discourse. The ... study examines which characteristics of peer-reviewed education research predict...using a standardized coding manual + Extract and record study characteristics including methodology, sample features, topic areas, and… more
- Bon Secours Mercy Health (Toledo, OH)
- …- Attaches electrodes and other recording devices to patients undergoing sleep studies according to standardized procedures. Removes and cleans all such devices at ... the completion of sleep study . **30%** - Monitors PSG collection computers and make...**20%** - Titrates PAP devices and O2 during sleep study for optimal resolution of respiratory events and nocturnal… more
- Boehringer Ingelheim (Ridgefield, CT)
- …delivery team, liaising closely with the Clinical Trial Managers ("CTM") on all study -related issues. As leader of the Trial Team, the SR AD, CTL communicates ... trial level documents owned by other functions (eg, Statistics, Data Management, Study Physician, Medical Writing, Site Monitoring). + Verifies and provides input… more
- Defense Logistics Agency (Pearl Harbor, HI)
- …unusual problems, and significant issues requiring management decisions. Conducts in-depth studies on staffing and productivity and works with management to ... your graduate school has determined to represent one academic year of full-time study . Such study may have been performed on a full-time or part-time basis. If… more
- Johns Hopkins University (Baltimore, MD)
- …with general duties in Dr. Quiros-Alcala's Research Laboratory and assists with a study to better understand work exposures among Black and Latina hair salon ... + Assist with collection and organization of data per study requirements, eg participant interviews, administer questionnaires, conduct background research,… more
- Teva Pharmaceuticals (Miramar, FL)
- …ensuring timely, accurate, and comprehensive processing during screening, admission, study conduct, and discharge procedures. **Essential Functions** * Performs ... COVID-19 testing, etc.) and processes in strict compliance with the study protocol, Good Clinical Practice (GCP) standards, Standard Operating Procedures (SOPs),… more
- IQVIA (Durham, NC)
- …line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with ... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and… more
- Cedars-Sinai (Los Angeles, CA)
- …a Clinical Research Coordinator II, you will work independently providing study coordination including screening of potential patients for protocol eligibility, ... CRC II member will be responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other… more
- HCA Healthcare (Chattanooga, TN)
- …assistants or other delegates of the Principal Investigator. Coordinates and manages clinical studies according to OHRP and FDA regulations, as well as ICH Good ... to private industry or governmental sponsors of clinical trials. Assists in preparing study contracts and budgets. Obtain detailed knowledge of all components of … more