- University of Colorado (Aurora, CO)
- …IND or IDE. **Additional Preferred Qualifications for RAC III** + Working knowledge of FDA Regulations and OHRP Guidance - how they apply to oncology clinical ... **Regulatory Affairs Coordinator (Open Rank: Entry/Level 1 Senior/Level 3)** **Description**...and/ or Investigator initiated clinical trials in accordance with FDA Regulations , Good Clinical Practice (GCP) and… more
- University of Pennsylvania (Philadelphia, PA)
- …of Pennsylvania, FDA and GCP guidelines. Job Description Clinical Research Coordinator BWith minimal supervision, the Clinical Research Coordinator at Level ... regulations + Position contingent upon funding Clinical Research Coordinator C + Bachelor's degree and a minimum of...multidisciplinary teams and sponsors + In-depth knowledge of IRB regulations , FDA guidelines, and GCP standards +… more
- University of Colorado (Aurora, CO)
- …**Preferred Qualifications:** + Experience working with Institutional Review Boards or OHRP/ FDA regulations regarding human subject research + Certified IRB ... **IRB Panel Coordinator ** **Description** **University of Colorado Anschutz Medical Campus**...Human Research Protections (OHRP) and Food and Drug Administration ( FDA ) regulations for human subject research +… more
- LSI Solutions (Victor, NY)
- …seeking a person who is highly organized and detail-oriented to become a Regulatory Coordinator to support the smooth operation of our department. In this role, you ... right candidate to transition into the world of regulatory. POSITION TITLE: Regulatory Coordinator HOURLY PAY RANGE: $25.00 - $28.00 POSITION HOURS: 8:00AM - 5:00PM… more
- University of Utah (Salt Lake City, UT)
- …relations and effective communication skills also required. Knowledge of Good Clinical Practices, FDA , HIPAA and IRB regulations ; an understanding of research ... the study. 6. Prepares, submits, and maintains IRB , FDA , NCI , NIH , NSF , HRSA...regulations may be referred to the Title IX Coordinator , to the Department of Education, Office for Civil… more
- Stanford University (Stanford, CA)
- …research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations , Institutional Review Board requirements, and Good Clinical ... Senior Research Coordinator in Precision Psychiatry and Neuroimaging **School of Medicine, Stanford, California, United States** **New** Research Post Date 2 days… more
- University of Utah (Salt Lake City, UT)
- …hematology or oncology trials. + Demonstrated knowledge of ICH - GCP , FDA regulations , and clinical trial lifecycle. + Strong documentation, organizational, and ... SOPs, Good Clinical Practice ( GCP ), and applicable regulations ( FDA , ICH , NIH...regulations may be referred to the Title IX Coordinator , to the Department of Education, Office for Civil… more
- Tecomet (Woburn, MA)
- …and updates of product and process-related data in accordance with internal procedures, FDA regulations , and ISO requirements. + Supports internal and external ... **TITLE** : Document Control Coordinator **JOB SUMMARY:** Responsible for leading a structured,...records to ensure documentation procedures are maintained based on FDA /ISO and Corporate standards and regulations . **ESSENTIAL… more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C Job Profile Title Clinical Research Coordinator B Job ... ACC. The ACC CRU Leukemia Research Team seeks a full-time Clinical Research Coordinator to organize, coordinate and implement complex cancer studies involving a wide… more
- MD Anderson Cancer Center (Houston, TX)
- …* Observe and support the assembly of regulatory documents per local and FDA regulations , institutional SOPs, and clinical trial processes (eg, study activation, ... * Coordinator , Clinical Research Regulatory - Leukemia* *MISSION STATEMENT*...files and documentation. * Ensure compliance with all applicable regulations , guidelines, and standards (eg, FDA , GLP).… more