- Abbott (Minneapolis, MN)
- …Contracts Associate), as needed. Manage all aspects of study lifecycle to include site regulatory and quality: + Start Up + Nominate, approach, and complete ... aspects of the start -up process and site initiation visits + Understand regulatory and legal requirements for study participation at a level that allows for… more
- Abbott (Pleasanton, CA)
- …as needed. **2. Manage all aspects of study lifecycle to include site regulatory and quality:** Start Up + Nominate, approach, and complete qualification ... aspects of the start -up process and site initiation visits + Understand regulatory and legal requirements for study participation at a level that allows for… more
- University of Washington (Seattle, WA)
- …supervises and partners closely with teams responsible for fiscal management, regulatory affairs, trial start -up, and research coordination. Through strategic ... of research procedures to promote consistency, streamline operations, and ensure regulatory compliance. This position ensures that all research activities, grants,… more
- IQVIA (Parsippany, NJ)
- Essential Functions * Assist Clinical Research Associates (CRAs) and Regulatory and Start -Up (RSU) team with accurately updating and maintaining clinical ... coworkers, managers, and clients. * Awareness of applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference… more
- Parexel (Richmond, VA)
- …investigators. + In some countries, as required, CRAs are accountable for study start -up and regulatory maintenance. Tasks may include Site Qualification Visits, ... application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start -up and for the duration of the study. + Trains,… more
- Parexel (Columbus, OH)
- …+ In some countries, as required, SrCRAs are accountable for study start -up and regulatory maintenance. Tasks may include Site Qualification Visits, ... application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start -up and for the duration of the study. + Trains,… more
- University of Pennsylvania (Philadelphia, PA)
- …and processing regulatory documents for submission to the IRB, and all regulatory committees from study start -up to completion. Interact with study sponsors, ... regulatory documents for submission to the IRB, and all regulatory committees from study start -up to completion. Data transfer and collection of imaging data… more
- AKS Engineering & Forestry (Keizer, OR)
- …team of scientists, planners, and engineers and help our clients navigate complex regulatory requirements from start to finish. What You'll Do + Conduct ... federal permit applications, reports, and/or memos associated with environmental and regulatory compliance. + Coordinate with state, local, and federal agencies to… more
- Parexel (Bismarck, ND)
- …with CRA for enrollment delivery during study conduct + Partners with local Regulatory authorities and Study Start up teams to ensure timely completion ... investigative sites throughout a study's lifecycle, responsible for site start -up, activation, relationship management, recruitment, and quality assurance. This role… more
- HCA Healthcare (Hermitage, TN)
- …contrast media and medications according to age- and weight-specific guidelines and within regulatory scope. . Start and maintain IV access; monitor patients ... before, during, and after procedures, reporting any abnormalities. . Prepare patients by reviewing their medical history, positioning them, and prepping procedure sites. . Operate and maintain imaging and lab equipment; report malfunctions and follow… more