- Cellectis (New York, NY)
- …development team meetings as required. In collaboration with Data Management/Programming develop Data Review Plan, and monitor clinical data for specific ... of clinical contributions to internal documents and presentations for assigned studies ; including clinical study reports (CSRs) and clinical… more
- The University of Chicago (Chicago, IL)
- …(GCP). Ability to read and understand clinical trials protocols. Understanding of the IRB submission and review process and when and how to apply for ... the compliance, financial and other related aspects of the clinical study . Responsibilities Research Conduct/ Study ...IRB review . Understanding of the federal research… more
- Cellectis (New York, NY)
- …in conjunction with pharmacovigilance in collaboration with Data Management will develop Data Review Plan, and monitor clinical data for specific trends, ... & implementation of clinical trial(s), their delivery, clinical data review and data cleaning, interpretation...or other appropriate forums, act as primary point-of-contact for clinical study or program for clinical… more
- University of Iowa Hospitals & Clinics (Iowa City, IA)
- …of the appropriate Human Subjects Review forms and application materials to the Institutional Review Board ( IRB -01) as well as external IRBs ... oversight and management of multiple complex clinical studies . Serve as a liaison with IRB ... IRB staff, regulatory authorities, and investigators and study coordinators. Coordinate external and internal review … more
- Planned Parenthood (Minneapolis, MN)
- …of the Research Manager. This position will focus on research study start-up, Institutional Review Board ( IRB ) submissions, study project ... of experience in clinical research, including coordinating clinical research studies from start up to...Study Coordination and Reporting Independently develop and prepare Institutional Review Board applications, including… more
- The University of Pennsylvania (Philadelphia, PA)
- …and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and assist in ... to procedures as needed and monitor results. Responsible for study coordination for investigator-initiated studies , multi-center research studies ,… more
- Children's National Hospital (Washington, DC)
- …the development of action plans to improve quality. Facilitates the preparation of Institutional Review Board applications for research proposals, develops ... related information per federal regulations/ICH guidelines, GCPs, SOPs, sponsor/CRO and IRB requirements. Oversee subject recruitment and study enrollment goals.… more
- Indiana University (Indianapolis, IN)
- …critically evaluates, and comments upon study contracts/agreements. Prepares and submits Institutional Review Board ( IRB ) documents (ie, Informed ... staff regarding scientific aspects of study and trains ancillary staff regarding clinical studies or trials; monitors study team compliance with required… more
- Insight Global (New York, NY)
- …Site Management, you will manage the day-to-day operations of assigned study components, ensuring the successful implementation of project deliverables and adherence ... training materials. You will provide necessary training to sites, coordinate IRB submissions, and maintain regulatory documentation. Additionally, you will manage… more
- Syneos Health Careers (Morrisville, NC)
- …Protect the safety of human subjects. Monitor appropriate sources for specific clinical study or federal regulation updates. Collect and enter study ... timeframe . Monitor appropriate sources for specific clinical study or federal regulation updates. Complete... monitor , CRF, or other internal/external findings . Review and/or oversee close-out of study documentation,… more
- Actalent (Indianapolis, IN)
- … Research Coordinator, you will serve as the primary coordinator for clinical research studies , responsible for enrolling patients, creating source ... data, creating data report forms, and maintaining communication with study sponsors. You will lead 3-5 studies ...Prepare and process laboratory specimens for shipment according to study protocols. Review laboratory and ancillary tests,… more
- HEALTH FEDERATION OF PHILADELPHIA (Philadelphia, PA)
- …in Philadelphia; working with the medical community to improve reporting, clinical , and prevention activities; promoting best practices for people who have ... and oversee production of regular reports on viral hepatitis data to monitor progress towards program goals. Coordinate with other Epidemiologists to execute program… more
- University of Utah (Salt Lake City, UT)
- …or knowledge of oncology, and oncology related research + Prior experience with Institutional Review Board ( IRB ) procedures + Strong written and oral ... assurance reviews, including monitor and audit visits on cancer related clinical trials to ensure compliance with study protocol, University, state and… more
- Alaka'ina Foundation Family of Companies (Camp Lejeune, NC)
- Institutional Review Board Administrative...the IRB Chairman and is accountable for IRB administrative matters to the Clinical Investigation ... Family of Companies (FOCs) is possibly looking for an Institutional Review Board Administrative Support...and serve as a resource, to co-workers in the IRB office. + Monitor the regulatory environment… more
- Alaka'ina Foundation Family of Companies (Silver Spring, MD)
- …training and education programs + Experience compiling and auditing clinical study packages for IRB review + Experience monitoring/auditing ... determinations. Verify the appropriate regulations are applied during the review of a study and validate that...EXPERIENCE: + Minimum three (3) years experience as a Clinical Trial Monitor + Knowledge and experience… more
- UTMB Health (Galveston, TX)
- … Research Monitor or Coordinator experience + Experience with a Clinical Trial Management System (CTMS), electronic IRB platform and EMR **LICENSES, ... Coach is to provide mentorship, instruction and guidance to clinical research investigators, nurses, coordinators, and other study...study visits to provide support and feedback. 6. Review initial study documentation to ensure it… more
- Touro University (Hawthorne, NY)
- … team. + Ensure compliance with the Good Clinical Practice guidelines in clinical research. + Monitor study patients for adverse events in collaboration ... institutional protocols. + Screen and enroll patients onto clinical trials in collaboration with clinical team,...mail, phone, fax, e-mail for COG, sponsored, local and multi- institutional studies . Act as liaison between NYMC… more
- Children's Hospital Los Angeles (Los Angeles, CA)
- …all aspects of research protocols and clinical trials. Monitor study patients and provide appropriate nursing services; review and evaluate health ... care that is personal, convenient and empowering. Our scientists will work with clinical experts to take laboratory discoveries and create treatments that are a… more
- Novant Health (Winston Salem, NC)
- …under the direction of their Novant Health leader in conjunction with study investigators. Clinical Research Coordinators facilitate and coordinate daily ... play a critical role in the conduct of the study . Our Clinical Research Coordinators are dedicated...clinical trial related activities. Collects, enters and summarizes clinical trial data. Monitor patients, their results,… more
- University of Colorado (Aurora, CO)
- …and oversee the day to day operations of clinical trials and studies + Obtain study subject's medical history and current medication information, reviews ... not move beyond this level.** This position will coordinate clinical research studies for the Depression and... study progress summaries for sponsors, independent site monitor for clinical trials, and independent monitoring… more
