- University of Michigan (Ann Arbor, MI)
- …the Fast Forward Medical Innovation, the Biomedical Research Core Facilities (BRCF), the Institutional Review Board (IRBMED), and the Medical School Grant ... Senior Associate Regulatory Analyst Apply...position our researchers for success. The mission of the Institutional Review Board of the Medical… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …With guidance from senior team member, proficiently facilitates and documents IRB Committee Meetings according to institutional and IRB policies ... regulations. + Screens and processes continuing review applications according to institutional and IRB policies and procedures and federal regulations. +… more
- Boston University (Boston, MA)
- …Maintains documentation in accordance with Federal regulations and institutional policies. The Senior IRB Analyst can, at the direction of the ... The Sr. IRB Analyst provides administrative and regulatory support...Amendments, Deviations, AEs and Exceptions.) Prepares protocols for full Board review at IRB meetings… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …ethical and regulatory compliance. Reporting to an Associate Director or Director, the Senior IRB /SRC Analyst is responsible for the supervision of OHRS ... CT)** Located within the Office for Human Research Studies (OHRS), the IRB /SRC Analyst job family is critical to the review and approval of research studies… more
- University of Miami (Miami, FL)
- …+ Prepare and coordinate the entire process of regulatory document submission to the Institutional Review Board ( IRB ) from study start-up to study ... has an exciting opportunity for a Full Time Remote Regulatory Analyst 1. The Remote SCCC ... regulatory documents. Maintains current knowledge of applicable regulatory topics (eg, institutional SOPs, federal regulations,… more
- University of Miami (Miami, FL)
- …to: Prepare and coordinate the entire process of regulatory document submission to the Institutional Review Board ( IRB ) from study start-up to study ... has an exciting opportunity for a Full Time Remote Regulatory Analyst 1. CORE JOB SUMMARY: The... regulatory documents. Maintains current knowledge of applicable regulatory topics (eg, institutional SOPs, federal regulations,… more
- Vitalief (New Brunswick, NJ)
- …+ Reporting to the Manager, Budget & Reimbursement, this financial analyst is responsible for preparing, maintaining, and negotiating budgets related to ... a qualifying trial per CMS regulations, and assesses compliance with other regulatory requirements, including FDA and NIH guidelines. + Negotiates budgets with… more
- Rush University Medical Center (Chicago, IL)
- …detailed and accurate coverage analyses with budget overlay in a timely manner. * Review clinical trial protocols and related regulatory documents in order to ... of related guidance and their effect on research billing processes. The analyst will provide high-level professional support in the growing efforts to conduct… more
- Rush University Medical Center (Chicago, IL)
- …detailed and accurate coverage analyses with budget overlay in a timely manner. * Review clinical trial protocols and related regulatory documents to prepare a ... of related guidance and their effect on research billing processes. The analyst will provide high-level professional support in the growing efforts to conduct… more
- MD Anderson Cancer Center (Houston, TX)
- The Senior Data Security Analyst position is to function as a resource that will contribute towards the development, implementation and maintenance of the ... emerging technologies. This resource will counsel interdepartmental personnel on institutional information security policies, regulatory compliance issues,… more
- Rush University Medical Center (Chicago, IL)
- …invoices from the vendors are received and accurate based upon agreed costs. * Review accuracy of the Clinical Research Coverage Analyst and Clinical Research ... Financial Analyst daily work. * Review / audit of daily activity of the Clinical Research...Cycle colleagues, study teams, patients, Office of Research Affairs, IRB , RUMC Compliance, and all partners in the Research… more
- Dana-Farber Cancer Institute (Boston, MA)
- …retrieval, labelling, and other preparation of the collation of biological specimens; regulatory needs such as User Committee proposals, IRB applications, ... serial blood samples with direction and guidance from the Senior Director and Associate Director of the overall Cohort...as directed/required by the protocol and/or study team. + Review and abstract clinical information from medical records for… more