- University of Pennsylvania (Philadelphia, PA)
- …study initiation; maintaining study regulatory binders; submission of all regulatory paperwork to our institutional review board ( IRB ) and any applicable ... overall research mission. Prepare draft PS-IDE applications for faculty review and submission to FDA. Draft components of clinical protocols and informed… more
- Bausch + Lomb (Harrisburg, PA)
- …(GCP), clinical trials management (including site monitoring), scientific methods, research design, regulatory compliance , and clinical data management. ... established over our 170-year history. We have a significant global research , development, manufacturing and commercial footprint of approximately 13,000 employees… more
- University of Pennsylvania (Philadelphia, PA)
- … compliance in one or more studies. Job Description Research coordinator work includes study implementation, document development, submission to regulatory ... or CRO, includes source documentation, case report forms, and research charts. Collect, review and report study...of a team, as well as independently; knowledge of IRB and human research protection regulations; high… more
- University of Pennsylvania (Philadelphia, PA)
- …clinical trials. + Prepare and process all regulatory documentation/applications through the IRB and requisite ancillary review committees. + Prepare and process ... the research at the site. + Participate in study team meetings, research team meetings, and ongoing protocol training/ compliance meetings. + Facilitate the… more
- University of Pennsylvania (Philadelphia, PA)
- …the Investigator, sponsor or CRO, includes source documentation, case report forms, and research charts. Collect, review and report study data. Complete case ... ability to work as part of a team, as well as independently; knowledge of IRB and human research protection regulations CRC-B Bachelor of Science and 2 to… more
- University of Pennsylvania (Philadelphia, PA)
- …also include: transporting specimens, submission of study documents to all applicable institutional committees (eg, IRB , CTSRMC, IBC, CHPS) for initial approval, ... private employer in Philadelphia, is a world-renowned leader in education, research , and innovation. This historic, Ivy League school consistently ranks among… more
- University of Pennsylvania (Philadelphia, PA)
- …private employer in Philadelphia, is a world-renowned leader in education, research , and innovation. This historic, Ivy League school consistently ranks among ... and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title Clinical Research Coordinator A Job… more
- University of Pennsylvania (Philadelphia, PA)
- …for regulatory documentation through the IRB , FDA and all applicable institutional regulatory review committees. In collaboration with clinical research ... Specialist post-site initiation. He/she will participate in regulatory staff meetings, research team meetings, and ongoing protocol training/ compliance meetings.… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …+ Oversee execution of Investigator Initiated Trials (IIT) and Collaborative Clinical Research (CCR) initiatives including governance of IIT review committees ... Global Clinical Lead, Digital and AI is a strategic leader within the Clinical Research leadership team, reporting directly to the Global VP, Clinical Research .… more
- Geisinger (Danville, PA)
- …and external stakeholders; this includes Geisinger groups such as clinical departments, the IRB , and the compliance , quality, and legal functions + Conducting ... Staff Scientist, Statistician, Project Manager). + Develops and leads research projects within the defined scope of the supervising...position may also be sent to the same address. Review of applications will begin immediately and will continue… more