- University of Pennsylvania (Philadelphia, PA)
- …collection, researching and writing animal protocols, preparing and submitting regulatory documentation, maintaining laboratory space, and ordering supplies. Job ... collection, researching and writing animal protocols, preparing and submitting regulatory documentation, maintaining laboratory space, and ordering supplies. Position… more
- University of Pennsylvania (Philadelphia, PA)
- …translational and clinical research, and clinical trials. Additionally, they manage regulatory submissions (IRB, IACUC, RIS) and directly support research activities ... translational and clinical research, and clinical trials. Additionally, they manage regulatory submissions (IRB, IACUC, RIS) and directly support research activities… more
- University of Pennsylvania (Philadelphia, PA)
- …multiple locations across the health system, biospecimen processing, and regulatory management. This position involves working directly with several Investigators ... of clinical trial databases using REDCap functionality. Maintain subject files and regulatory files per GCP. + Utilize Electronic Medical records to collect data… more
- University of Pennsylvania (Philadelphia, PA)
- …management of laboratory tools, documentation and processes to ensure regulatory compliance and timely completion of project/program deliverables. Excellent ... and immunochemistry. + Collect data and documentation to ensure regulatory compliance. + Assist with inventory and ordering of...allows you to relax, take vacations, attend to personal affairs , recover from illness or injury, spend time with… more
- University of Pennsylvania (Philadelphia, PA)
- …Conduct hands-on radiolabeling experiments in compliance with safety and regulatory standards. . Collaborate with interdisciplinary teams including synthetic ... Conduct hands-on radiolabeling experiments in compliance with safety and regulatory standards. . Collaborate with interdisciplinary teams including synthetic… more
- University of Pennsylvania (Philadelphia, PA)
- …PET image analysis, PET drug manufacturing, therapeutic drug synthesis and related regulatory guidelines as a member of a small, multidisciplinary research group. ... PET image analysis, PET drug manufacturing, therapeutic drug synthesis and related regulatory guidelines as a member of a small, multidisciplinary research group.… 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 ... I-IV clinical trials (10% Essential: 1),Prepare and process all regulatory documentation through the IRB, CTSRMC, FDA and all...allows you to relax, take vacations, attend to personal affairs , recover from illness or injury, spend time with… more
- University of Pennsylvania (Philadelphia, PA)
- …QC; study close out activities). + Develop, create and review regulatory submission and study documents/tools, including protocols, consents, annual reports, source ... writing assistance); and/or post award finance activities (invoicing, billing review). + Staff supervision: Assist and train direct and/or indirect research staff… more
- Bristol Myers Squibb (Princeton, NJ)
- …Strategy within WW Medical Cardiovascular & Immunology (CV & I) Global Medical Affairs , and is responsible for assisting with early medical and scientific strategy ... resource allocation and prioritization of projects. + Collaborate with R&D, Commercial, Regulatory , and other key functions to ensure seamless execution of portfolio… more
- Bristol Myers Squibb (Princeton, NJ)
- …acceptance criteria. + Prioritize and groom the backlog to balance regulatory compliance, business value, risk, and technical feasibility; run effective PI/iteration ... facilitating risk assessments. + Strong stakeholder leadership across Medical Affairs , Medical Information, Field Medical, Compliance/QA, Architecture, and Engineering;… more