- State of Massachusetts (Haverhill, MA)
- …ensuring effective data reporting for sponsor requirements. * Provide leadership to the Institutional Review Board (IRB) process _Ensure Ongoing and ... *PLEASE NOTE, WE DO NOT REVIEW APPLICATIONS SUBMITTED THROUGH MASSCAREERS. PLEASE APPLY VIA THE LINK BELOW:*… more
- Brown University (Providence, RI)
- …of the BIRCH initiative (http://birch.brown.edu/) , Brown will soon be the main HRPP and Institutional Review Board (IRB) of record for Brown, Lifespan and ... administration and implementation of the Human Research Protection Program (HRPP) and Institutional Review Board (IRB) policies and procedures related to the… more
- Texas A&M University System (Kingsville, TX)
- …regulations. This includes providing administrative and regulatory oversight for the Institutional Review Board (IRB), Institutional ... institutional policies. Export Control Compliance: + Assists with review of research activities for restrictions, technology control plans, international… more
- Henry Ford Health System (Southfield, MI)
- …informed consent processes, and human subjects protection principles. + Coordinate with the Institutional Review Board (IRB) to facilitate efficient ... Ford Health - Providence Hospital. The Director ensures compliance with institutional , regulatory, and ethical standards governing bothanimal and human subjects… more
- Centers for Medicare & Medicaid Services (Woodlawn, MD)
- …as a Member of the five Member Provider Reimbursement Review Board , which adjudicates adversarial disputes over institutional reimbursement matters in the ... accountants and attorneys, to fill a vacant position on the Provider Reimbursement Review Board (PRRB). The PRRB is an independent five-member panel that… more
- University of Southern California (Los Angeles, CA)
- …is performed as described in protocol. Serves as contact for subjects, study personnel, Institutional Review Board (IRB) and study sponsor. + Assists in ... of study continuing review and study amendments to Institutional Review Board (IRB). Assists investigators with reportable event submissions… more
- Stanford University (Stanford, CA)
- …Human Subjects Panel. + Coordinate new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies. Complete annual ... reports to Institutional Review Board , CSTA, FDA and other regulatory agencies. Submit Investigational New Drug applications to the FDA as required. + Audit… more
- Magellan Health Services (Falls Church, VA)
- …matter expert to Institutional Officials, Human Research Protections Officers (HRPOs), Institutional Review Board (IRB) members and staff, and other ... Specialist will assist with oversight of human research protection programs, Institutional Review Boards (IRBs), human subject protection standards, policy… more
- Stanford University (Stanford, CA)
- …community organizations. . Coordinate new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies. Complete annual ... reports to Institutional Review Board , CSTA, FDA and other regulatory agencies. Submit Investigational New Drug applications to the FDA as required. . Audit… more
- Cedars-Sinai (Los Angeles, CA)
- …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **Primary Duties and Responsibilities** + ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
- Cedars-Sinai (Beverly Hills, CA)
- …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **Primary Duties and Responsibilities** + ... conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
- Cedars-Sinai (Beverly Hills, CA)
- …forms (CRFs), entering clinical research data, and assisting with regulatory submissions to the Institutional Review Board (IRB). The CRA I member may have ... term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board (IRB) and works closely with supervising research staff… more
- Stanford University (Stanford, CA)
- …Human Subjects Panel. + Coordinate new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies. Complete annual ... reports to Institutional Review Board , CSTA, FDA and other regulatory agencies. Submit Investigational New Drug applications to the FDA as required. + Audit… more
- Cedars-Sinai (Beverly Hills, CA)
- …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Duties and Responsibilities + ... conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
- Cedars-Sinai (Beverly Hills, CA)
- …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **Primary Duties and Responsibilities** + ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
- Stanford University (Stanford, CA)
- …Human Subjects Panel. + Coordinate new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies. Complete annual ... reports to Institutional Review Board , CSTA, FDA and other regulatory agencies. Submit Investigational New Drug applications to the FDA as required. + Audit… more
- Cedars-Sinai (Los Angeles, CA)
- …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **Primary Duties & Responsibilities** + ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
- Cedars-Sinai (Los Angeles, CA)
- …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **Primary Duties and Responsibilities:** + ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
- Cedars-Sinai (CA)
- …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **Primary Duties & Responsibilities** + ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
- Cedars-Sinai (Los Angeles, CA)
- …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **Primary Job Duties and Responsibilities:** ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
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