- University of Pennsylvania (Philadelphia, PA)
- …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... protection + Other duties and responsibilities as assigned CRC-A + Prepare and process all Institutional Review Board ( IRB )through the IRB and… more
- University of Pennsylvania (Philadelphia, PA)
- …and flexible hours. Assist the regulatory specialist in preparing for all local and Central Institutional Review Board ( IRB ) documentation through the ... or more studies. This position is responsible for study coordination for investigator-initiated studies, multi-center research studies,...the FDA and other entities. Correspond regularly with the Institutional Review Board and other… more
- University of Pennsylvania (Philadelphia, PA)
- …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... to procedures as needed and monitor results. Responsible for study coordination for investigator-initiated studies, multi-center research studies, and… more
- University of Pennsylvania (Philadelphia, PA)
- …duties and responsibilities as assigned Regulatory Responsibilities: + Prepare and process all Institutional Review Board ( IRB ) documentation through the ... and retrospective observational studies. This position will report directly to the Research Nurse Manager and work directly with Physician Investigators on… more
- University of Pennsylvania (Philadelphia, PA)
- …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... employer in Philadelphia, is a world-renowned leader in education, research , and innovation. This historic, Ivy League school consistently...to all applicable PENN institutional committees for review and approval to start trial (eg, IRB… more
- University of Pennsylvania (Philadelphia, PA)
- …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... to procedures as needed and monitor results. Responsible for study coordination for investigator-initiated studies, multi-center research studies, and… more
- University of Pennsylvania (Philadelphia, PA)
- …Posted Job Title Research Project Manager B/C Job Profile Title Manager Research Project B Job Description Summary Job Description Research Project ... Manager will support junior faculty members in their research projects and assist with research endeavors...with effective time management and mature judgment. Knowledge of IRB and human research protection regulations is… more
- 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 ... Manager (Department of Surgery) Job Profile Title Clinical Research Program Manager C Job Description Summary...research mission. Prepare draft PS-IDE applications for faculty review and submission to FDA. Draft components of clinical… more
- University of Pennsylvania (Philadelphia, PA)
- …coordination of Phase I-V clinical trials. Reporting to the Regulatory Affairs Research Teams Manager , the Regulatory Affairs Specialist-CC will, with minimal ... supervision, prepare and process all regulatory documentation through the IRB , CTSRMC, FDA and all applicable regulatory review...of a team, as well as independently; knowledge of IRB and human research protection regulations, including… more
- University of Pennsylvania (Philadelphia, PA)
- …Will problem-solve the challenges to implement a plan of action. Work with the regulatory manager to ensure that submissions to the IRB are completed in a timely ... maintain all required documentation- including source documentation, case report forms, and research charts. Collect, review and report study data, Complete case… more