- BayCare Health System (Clearwater, FL)
- …and laws. + Acts as a liaison between the sponsor, Clinical Research Operations, Institutional Review Board and internal departments/ staff to complete ... initial Institutional Review Board protocol submissions. + Submit study amendments in a timely fashion including changes to the protocol, consent forms and… more
- University of Miami (Miami, FL)
- …+ Develop, review and submit required documentation to the UM/JMH IRB to ensure successful approval of research protocols. Maintain any reports and other ... faculty or staff position using the Career worklet, please review this tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . Clinical Research Coordinator… more
- University of Florida (Gainesville, FL)
- …the EEG data collection, organization, and preprocessing. This position includes IRB management, programming and running experiments; entering and processing data; ... experience with infants and children. Preferred qualifications include excellent IRB management and orgainizational skills, database management experience, experience… more
- University of Miami (Miami, FL)
- …staff position using the Career worklet, please review this tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . The ... for modifications and adverse responses. + Prepare NIH and IRB applications. + Assist in the development of recruitment...Ensure protocol is being followed as approved by the IRB . Participate in research activities by assisting in the… more
- Trinity Health (Fort Lauderdale, FL)
- …consent process, completion of case report forms, data clarification, IRB preparations, chart abstraction, hosting monitor visits, organizing site initiation ... these processes and for maintaining up to date knowledge on these policies from IRB , FDA, ICH, GCP, or other sources. Experience with cardiology clinical trials and… more
- University of Miami (Miami, FL)
- …staff position using the Career worklet, please review this tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . Biochemistry ... including: Monitoring study participant appointments Documenting study events in RedCap Review clinical provider schedules and screen patients in accordance with … more
- University of Miami (Coral Gables, FL)
- …2. Compliance & Reporting: + Ensure ongoing compliance with NIH regulations, IRB requirements, Good Clinical Practice (GCP), and institutional research policies. ... faculty or staff position using the Career worklet, please review this tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . CORE JOB SUMMARYThe… more
- University of Miami (Miami, FL)
- …staff position using the Career worklet, please review this tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . Project ... have significant clinical research, proficiency with working through a central IRB to coordinate regulatory approvals for multiple ongoing studies, outstanding… more
- University of Miami (Miami, FL)
- …staff position using the Career worklet, please review this tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . The ... consent. + Assists with the preparation and monitoring of IRB documents, administers clinical interviews, and coordinates all assessment...projects 14. Sets up regular meeting for team to review status of all projects 15. Keeps and active… more
- Norstella (Tallahassee, FL)
- …our solutions. + Ensure all work complies with relevant regulatory requirements (eg, IRB , EC, GCP) and data privacy standards. + Mentor junior project managers and ... of clinical trial operations, patient recruitment strategies, regulatory requirements ( IRB /EC), and GCP standards. + Proficiency in project management tools… more