- ICON Clinical Research (Downers Grove, IL)
- …laboratory data and adverse reactions, and immediately notifying investigators, sponsors and the Institutional Review Board , if indicated, of any unexpected ... Grove, IL Office-based ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment… more
- University of Maryland, Baltimore (Baltimore, MD)
- …contributes to the conduct of research . * Coordinates the preparation of Institutional Review Board ( IRB ) and Health Insurance Portability ... Cellular Therapy (BMT-CT) research team within the Clinical Research Management Office of the University...general administrative duties. * Assists in the preparation of Institutional Review Board ( IRB… more
- University of Pennsylvania (Philadelphia, PA)
- …Coordinator B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board ( IRB ) documentation through the ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator - A/B (Department of...regulatory specialist in preparing for all local and Central Institutional Review Board ( IRB… more
- Stanford University (Stanford, CA)
- …or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. + Knowledge ... Clinical Research Manager **School of Medicine,...+ Coordinate new protocol submissions, renewals, and revisions to Institutional Review Board for multiple… more
- Cedars-Sinai (Los Angeles, CA)
- …Assists with regulatory submissions to the Institutional Review Board ( IRB ) and works closely with supervising research staff or directly with the ... data, and assist with regulatory submissions to the IRB . Provides limited patient contact as needed for study...Institutional Review Board . Maintains research practices using Good Clinical Practice (GCP)… more
- Cedars-Sinai (Los Angeles, CA)
- …*Assists with regulatory submissions to the Institutional Review Board ( IRB ) and works closely with supervising research staff or directly with the ... data, and assist with regulatory submissions to the IRB . Provides limited patient contact with research ...Institutional Review Board . Maintains research practices using Good Clinical Practice (GCP)… more
- Cedars-Sinai (Los Angeles, CA)
- …with regulatory submissions to the Institutional Review Board ( IRB ) and works closely with supervising research staffor directly with the ... data, and assist with regulatory submissions to the IRB . Provides limited patient contact with research ...Institutional Review Board . Maintains research practices using Good Clinical Practice (GCP)… more
- AdventHealth (Orlando, FL)
- ** Clinical Research Coordinator II -RN -...regulations Serves as liaison between Principal Investigators and the Institutional Review Board ( IRB ... St, Orlando Fl 32804** **The role you'll contribute:** The Clinical Research Coordinator II RN (CRC-II RN)...+ Serves as liaison between Principal Investigators and the Institutional Review Board ( IRB… more
- Cedars-Sinai (Los Angeles, CA)
- …budget. + Perform Medicare coverage analysis for clinical trials and collaborates with Institutional Review Board ( IRB ) to finalize and obtain ... **Job Description** **Come join our team!** The Clinical Research Finance Coordinator I develops...including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB… more
- Cedars-Sinai (Los Angeles, CA)
- …for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... and Drug Administration (FDA) and local Institutional Review Board . + Maintains research practices using Good Clinical Practice (GCP) guidelines.… more
- Cedars-Sinai (Los Angeles, CA)
- …(FDA) and local Institutional Review Board . *Maintains research practices using Good Clinical Practice (GCP) guidelines. *Maintains strict patient ... skills with an organization known nationally for excellence in research !** The Clinical Research Associate...follow-up patients only. *Assists with regulatory submissions to the Institutional Review Board ( IRB… more
- University of Southern California (Los Angeles, CA)
- …Submits protocols and supporting documents to internal and external regulatory bodies (ie Institutional Review Board ), ensuring trials are consistent with ... and/or operations in the academic or private sector. Experience with submissions to the Institutional Review Board and/or the Federal Drug Administration for… more
- University of Pennsylvania (Philadelphia, PA)
- …directed by the supervisor. He/she will be responsible for submission of studies to Institutional Review Board ( IRB ), ongoing maintenance of regulatory ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator C (Department of Cardiovascular...each study. Assist with preparation and processing of all Institutional Review Board ( IRB… more
- Cedars-Sinai (Los Angeles, CA)
- …all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **_*This is a hybrid ... you have a passion for helping human kind?** The Clinical Research Coordinator I will work with...closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB… more
- Cedars-Sinai (Los Angeles, CA)
- …contact for long-term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of ... and Drug Administration (FDA) and local Institutional Review Board . + Maintains research practices using Good Clinical Practice (GCP) guidelines.… more
- Cedars-Sinai (Los Angeles, CA)
- …(FDA) and local Institutional Review Board . *Maintains research practices using Good Clinical Practice (GCP) guidelines. *Maintains strict patient ... **Job Description** **Key Job Responsibilities** The Clinical Research Associate I works directly...follow-up patients only. *Assists with regulatory submissions to the Institutional Review Board ( IRB… more
- Cedars-Sinai (CA)
- …for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... and Drug Administration (FDA) and local Institutional Review Board . + Maintains research practices using Good Clinical Practice (GCP) guidelines.… more
- Cedars-Sinai (Beverly Hills, CA)
- …for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... and Drug Administration (FDA) and local Institutional Review Board . + Maintains research practices using Good Clinical Practice (GCP) guidelines.… more
- University of Pennsylvania (Philadelphia, PA)
- …samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and assist ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator A/B (Department of Surgery...and collection of clinical data. Assist with Institutional Review Board ( IRB… more
- University of Pennsylvania (Philadelphia, PA)
- …Independently manage different phases of clinical trials. They may assist with Institutional Review Board ( IRB ) filings, sponsor and investigator ... phases of clinical trials. They may assist with Institutional Review Board ( IRB ) filings, sponsor and investigator filings and research related… more