- Children's Hospital Los Angeles (Los Angeles, CA)
- …Subjects Protection Program in the areas of protocol reviews, liaison with the Institutional Review Board , and simple to moderately complex correspondence. ... **Minimum Qualifications/Work Experience:** 1+ years IRB experience. **Education/Licensure/Certification:** Bachelor's degree in a scientific or business discipline… more
- WCG Clinical (Cary, NC)
- …of documents, client reporting and problem resolution. This position will: + Support the Board and clients by preparing documents for review in accordance with ... WCG IRB Operations Specialist (Remote) **General Information** **Organization:** WCG IRB **Job Type:** Full Time - Regular **Description and Requirements**… more
- Stony Brook University (Stony Brook, NY)
- …correspond with various internal and external constituents including sponsors, cooperative groups, Institutional Review Board and regulatory agencies. + May ... review (ie Cerner Powerchart). Experience working with an IRB (Investigational Review Board ) for research protocol submissions, amendments and reviews.… more
- Stony Brook University (Stony Brook, NY)
- …Act (HIPAA) and institutional regulations (eg, regulations pertaining to the Institutional Review Board ( IRB ). Demonstrated knowledge of ... Manage the end-to-end process for data sharing related agreements including initial review of agreement and IRB submission/approval, negotiation, execution, and… more
- Jobleads-US (Sunnyvale, CA)
- …consent to research conducted by 23andMe which is overseen by an independent third-party Institutional Review Board ( IRB ) regulated under the Common ... reflects the scale of our ambitions. From high-net-worth individuals to institutional funders, you'll develop and steward relationships that bring in significant,… more
- Oregon State University (Baker City, OR)
- …regulations under Family Educational Rights and Privacy Act ( FERPA ), Institutional Review Board ( IRB ) and OSU Youth Safety Guidelines. + Use multiple ... as the transfer process), careers, and trade and technical institutional support, and to strengthen community vitality The OSU...veteran, and other protected status. OSU will conduct a review of the National Sex Offender Public website prior… more
- Stony Brook University (Stony Brook, NY)
- …duties: + Review all active protocols, manage clinical trials from IRB initiation to close-out. + Sponsor's monitoring visits, and responsible for drug/device ... Emergency Medicine patients. + Submit pharmaceutical proposals and consent forms to the IRB . + Liaison between SBMC, pharmaceutical sponsor, patient and IRB . +… more
- Primastep LLC (Arlington, VA)
- …DON IRB -approved studies. Regulatory Documentation & Assurance Packages Prepare, review , and submit Federalwide Assurance (FWA) and DoD Assurance packages for ... and sponsored institutions engaged in human subjects research. Incident Review & Corrective Action Investigate unanticipated problems and noncompliance issues… more
- Primastep LLC (Arlington, VA)
- …refine, and manage project management tools to support an agency-wide HRPP. Review and assess compliance among agency components, labs, and external partners with ... both federal and agency-specific human subject research regulations. Prepare and review Federalwide Assurances (FWAs) and DoD Assurance packages for internal and… more
- Stony Brook University (Stony Brook, NY)
- …of patient eligibility for protocol participation by way of chart review , data collection and patient evaluation/assessment identification. In addition, the ... reporting all adverse drug reactions to the FDA, NCI, Oncology cooperative groups, IRB and sponsoring drug companies. Lastly, they will conduct patient and staff… more
- Seattle Children's (Seattle, WA)
- …and possess strong communication skills. The candidate should be familiar with IRB and other regulatory processes and assist with creating and maintaining regulatory ... documents; recruiting, consenting, and tracking study participants across all sites; organizing protocol implementation; and conducting routine monitoring. **Required Education and Experience** Bachelor's Degree in related discipline, or equivalent combination… more
- Carnegie Mellon University (Pittsburgh, PA)
- …supports research compliance requirements on supported awards includinghuman subjects ( IRB ) and animal (IACUC) protocols, clinical trials, export controls, andother ... compliance related requirements. + Program support may include supporting calls for projects by creating online submissionforms, assisting with coordinating web presence for specific programs, and point ofcontact for submissions, initial reviews and… more
- Stanford Health Care (Palo Alto, CA)
- …initiation visits. + Supports practices relating to pharmacy dispensing based on IRB approved clinical trials. + Provides guidance to investigational drug service ... major contraindications and potential side effects. **Licenses and Certifications** + CA Board of Pharmacy License - Registered Pharmacist required . and + BLS… more
- Stanford Health Care (Pleasanton, CA)
- …the supervising physician, enrolls patients in investigational studies approved by the Investigational Review Board ( IRB ), and orders the necessary tests and ... Hospital and Clinics (SHC) Medical Executive Committee and the SHC Board Credentials, Policies and Procedures Committee. **Locations** Stanford Health Care **What… more
- Carnegie Mellon University (Pittsburgh, PA)
- …supporting research compliance requirements on supported awards, including human subjects ( IRB ) and animal (IACUC) protocols, clinical trials, export controls, and ... other compliance-related requirements. + Review technical information from all project teams, attend technical project meetings, reviewing submissions from project… more
- Stanford Health Care (Palo Alto, CA)
- …the supervising physician, enrolls patients in investigational studies approved by the Investigational Review Board ( IRB ), and orders the necessary tests and ... Stanford Hospital and Clinics (SHC) Medical Executive Committee and the SHC Board Credentials, Policies and Procedures Committee. This job description covers all… more
- Carnegie Mellon University (Pittsburgh, PA)
- …supporting research compliance requirements on supported awards, including human subjects ( IRB ) and animal (IACUC) protocols, clinical trials, export controls, and ... other compliance-related requirements + Provide technical support for all aspects of the program, including reviewing technical information from all project teams, attending technical project meetings, reviewing submissions from project teams to ensure… more
- Stanford Health Care (Palo Alto, CA)
- …+ Manages the consent process to ensure it is performed in compliance with institutional , FDA, IRB , clinical trial sponsor and other applicable regulations. + ... scanned timely into the medical record and aligns with institutional and sponsor processes for the clinical trial. +...site visits and study close-outs; and collaborates on the review of documentation during protocol audits. + Develops protocol… more
- Stanford Health Care (Palo Alto, CA)
- …the supervising physician, enrolls patients in investigational studies approved by the Investigational Review Board ( IRB ), and orders the necessary tests and ... Hospital and Clinics (SHC) Medical Executive Committee and the SHC Board Credentials, Policies and Procedures Committee. **Locations** Stanford Health Care **What… more
- Terumo Medical Corporation (Somerset, NJ)
- …Sales as well as external stakeholders, to include FDA, NB, PMDA, KOL, HCP, IRB and publishers. The salary range for this position is $114,640 - $143,300 based ... Sales & Marketing organizations. + Contribute to development and review of risk and benefits of Terumo devices. +...risk and benefits of Terumo devices. + Create and/or review product claims based on the existing clinical and… more
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