- 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
- Houston Methodist (Houston, TX)
- …laws, regulations, guidance, policy and procedure developed by Houston Methodist Research Institute Institutional Review Board ( IRB ), Food and Drug ... study personnel. + Acts as a liaison between the institutional review committees, regulatory agencies, and the...+ Assists in the preparation of research protocols for IRB submission, submitting protocol amendments, preparing renewals,… more
- Stony Brook University (Stony Brook, NY)
- …Investigational New Drug (IND) and Investigational Device Exemption (IDE) applications. + Creating Institutional Review Board ( IRB ) submissions and ... Investigator Initiated Trial Specialist - Clinical Trials **Position Summary** The Cancer...managing correspondence across research sites, particularly in single- IRB /multi-site studies. + Planning and implementing changes to the… more
- University of Maryland, Baltimore (Baltimore, MD)
- …position significantly contributes to the conduct of research. * Coordinates the preparation of Institutional Review Board ( IRB ) and Health Insurance ... Maryland, Baltimore (UMB) is currently seeking a Clinical Research Specialist .* Accomplishes responsibilities by applying specialized and theoretical knowledge,… more
- Vanderbilt University Medical Center (Nashville, TN)
- …Research Staff Council monthly meetings. + Attends in-services advertised by the Institutional Review Board , Research Support Services, professional ... prepares and processes new IRB research proposals, amendments, continuing review applications and adverse events according to institutional and departmental… more
- Cedars-Sinai (Los Angeles, CA)
- …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties and ... and collaborative, multi-site clinical research. The CCC Clinical Research Specialist II will serve in a cross-functional role and...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
- Banner Health (Mesa, AZ)
- …through interactions with research staff, internal and external investigators, study sponsors and Institutional Review Board ( IRB ). 8. Participates in ... last for many years. As a **RN Clinical Research Specialist ** you play a crucial role in clinical trials,...of research, including patient care, data collection, and study protocol adherence. **Schedule:** Full-time, exempt, 40hrs week. Monday -… more
- Methodist Health System (Dallas, TX)
- …the IRB . * Create and/or adapt clinical trial informed consent documents for Institutional Review Board ( IRB ) submission. * Maintain regulatory ... Shift :** **Job Description :** Your Job: The Regulatory Specialist will perform expertise in the regulatory component of...events in accordance with Food and Drug Administration, sponsor protocol , and IRB regulations and guidelines. *… more
- Johns Hopkins University (Fort Defiance, AZ)
- …and regulations, and institutional policies that must be corrected prior to IRB review . + Determine that appropriate protocol and application-specific ... a **_Sr. Compliance Monitoring Specialist_** . There are several Institutional Review Boards (IRBs) that we report...the FDA or commercial sponsors. + Assist in the review of IRB action outcomes, including the… more
- Banner Health (Sun City, AZ)
- …through interactions with research staff, internal and external investigators, study sponsors and Institutional Review Board ( IRB ). 8. Participates in ... a safe and ethical manner, while ensuring compliance to the FDA and institutional regulations. **Schedule** : Monday - Friday 8am-5pm, This position will primarily… more