- George Washington University (Washington, DC)
- …The IRB Analyst I reports to the Associate Director and serves as a Institutional Review Board ( IRB ) resource person for IRB transactions. ... all GW Principal Investigators and other GW researchers. Conducts pre- IRB review of minimal risk research...Office Vice President of Research (OVPR) Family Research Administration Sub-Family Research Compliance … more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe role is accountable for performance and compliance for assigned protocols and sites in a country.Under the oversight of the CRA manager or CRD, ... the person ensures compliance of study conduct with ICH/GCP and country regulations,...and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …The Position Drives the understanding & delivery of quality clinical research (patient safety, rights & wellbeing; data reliability; scientific integrity; regulatory ... & process compliance . Takes ownership to deliver upon near-term North America...Novo Nordisk (eg, clinical trial site staff, IRBs, clinical research vendors). Manages relationships with multiple internal stakeholders relevant… more
- George Washington University (Washington, DC)
- …Safety (ORS) teams; Oversees the administrative, regulatory, and programmatic activities of the Institutional Review Boards ( IRB ); Institutional Animal ... OVERVIEW Job Description Summary: The Director, Regulatory Oversight position reports to the Associate Provost Research Integrity and Compliance (AP-RIC) and… more
- Middlebury College (Middlebury, VT)
- …$26.32-32.91 per hour. Core Responsibilities: + Provides direct support to the college's Institutional Review Board ( IRB ), managing protocol submissions ... requests for information and forwarding messages on for further review , as necessary. + Schedules and coordinates IRB...needed to secure approval, under the direction of the Associate Directot for Research Compliance .… more
- Stanford University (Stanford, CA)
- Sr. Institutional Review Board ( IRB ) Manager **Dean of Research , Stanford, California, United States** **New** Compliance Legal Post Date 3 days ... direction of the HRPP Associate Director and IRB Chair,you will conduct in-depth protocol review ... Participant **In addition, our preferred requirements include:** + ** Institutional Review Board professional certification.**… more
- Stanford University (Stanford, CA)
- Institutional Review Board ( IRB ) Manager **Dean of Research , Stanford, California, United States** Compliance Legal Post Date Jan 26, 2024 ... direction of the Associate Director and the IRB Chair, you will conduct in-depth protocol review...relevant experience. **In addition, our preferred requirements include:** + Institutional Review Board professional certification… more
- Guidehouse (Bethesda, MD)
- …track and review adverse event files and report events in accordance with Institutional Review Board ( IRB ) processes and policies. + Assist ... adverse event files and prepare reports in accordance with Institutional Review Board ( IRB...Clinical Research Coordinator (CCRC), or Certified Clinical Research Associate (CCRA) + Liaising with regulatory… 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 ... education for other Clinical Research Associates. Ensures compliance with all federal, local, FDA, IRB ,...and Drug Administration (FDA) and local Institutional Review Board . Maintains research practices… 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 ... excellence in research !** **Job Summary:** The Clinical Research Associate I works directly with a...and Drug Administration (FDA) and local Institutional Review Board . Maintains research practices… more
- Cedars-Sinai (Beverly Hills, CA)
- …Assists with regulatory submissions to the Institutional Review Board ( IRB ) and works closely with supervising research staff or directly with the ... **Job Description** The Clinical Research Associate I works directly with...and Drug Administration (FDA) and local Institutional Review Board . Maintains research practices… more
- Cedars-Sinai (Los Angeles, CA)
- …forms (CRFs), entering clinical research data, and assisting with regulatory submissions to the Institutional Review Board ( IRB ). The CRA I may have ... bio-specimens from patients for high quality basic and translational research . As a Clinical Research Associate...patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB… more
- Cedars-Sinai (Los Angeles, CA)
- …forms (CRFs), entering clinical research data, and assisting with regulatory submissions to the Institutional Review Board ( IRB ). The CRA I may have ... you to consider this phenomenal opportunity!** **As a Clinical Research Associate I, you will work directly...supervising research staff or directly with the Institutional Review Board to submit… 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 ... study budget and patient research billing. Ensures compliance with all federal, local, FDA, IRB ,...and Drug Administration (FDA) and local Institutional Review Board . + Maintains research … 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 ... study budget and patient research billing. Ensures compliance with all federal, local, FDA, IRB ,...and Drug Administration (FDA) and local Institutional Review Board . *Maintains research practices… 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 ... study budget and patient research billing. Ensures compliance with all federal, local, FDA, IRB ,...and Drug Administration (FDA) and local Institutional Review Board . *Maintains research practices… 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 ... study budget and patient research billing. Ensures compliance with all federal, local, FDA, IRB ,...and Drug Administration (FDA) and local Institutional Review Board . + Maintains research … 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 ... study budget and patient research billing. Ensures compliance with all federal, local, FDA, IRB ,...and Drug Administration (FDA) and local Institutional Review Board + Maintains research … more
- Loyola University Chicago (Chicago, IL)
- …Human Subjects ( IRB ). Secondary responsibilities include assisting the Associate Director of Research Compliance . Essential duties and responsibilities ... regulations requires administrative support of the chairperson of the Institutional Review Board for the...regulatory agency/department or internal reports as requested by the Associate Director of Research Compliance .… 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 ... study budget and patient research billing. Ensures compliance with all federal, local, FDA, IRB ,...and Drug Administration (FDA) and local Institutional Review Board . + Maintains research … more
