- UPMC (Carlisle, PA)
- …a disease-specific centers model for conducting clinical trials, CRS provides study development and implementation assistance, submissions to the FDA, IRB ... processing, patient recruitment, study coordination, study -specific training, data collection, and specimen collection and processing. UPMC Hillman Cancer Center… more
- UPMC (Pittsburgh, PA)
- …compliance with institutional and federal guidelines. This role works closely with study team and managers to ensure all protocol-required procedures are accurately ... + Reconcile payments based on subject visit tracking and study milestones + Ensure compliance with institutional policies and...+ Develop financial reports and forecasting tools to support study teams + Assist with affiliate and subaward payments… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- …high-quality standards throughout the clinical development lifecycle. **Key Responsibilities** **Clinical Study Support** + Serve as a GCP quality resource to ... clinical teams during study planning, conduct, and close-out. + Support the review...planning, conduct, and close-out. + Support the review of study documents (eg, protocols, monitoring plans, vendor agreements) for… more
- University of Pennsylvania (Philadelphia, PA)
- …schedule lab meetings + Manage select team members and coordinate the entire study team + Recruit, schedule and run research subjects; execute subject payments. + ... Assist with IRB prep and grant prep. + Order supplies and maintain study databases; maintain lab documentation for best practices, publications, update website, etc.… more
- Defense Logistics Agency (Philadelphia, PA)
- …hours that your graduate school has determined to represent one academic year of full-time study . Such study may have been performed on a full-time or part-time ... your graduate school's definition of one year of graduate study , 18 semester hours (or 27 quarter hours) should...satisfying the requirement for one year of full-time graduate study . FOREIGN EDUCATION: If you are using education completed… more
- Defense Logistics Agency (Philadelphia, PA)
- …hours that your graduate school has determined to represent one academic year of full-time study . Such study may have been performed on a full-time or part-time ... your graduate school's definition of one year of graduate study , 18 semester hours (or 27 quarter hours) should...satisfying the requirement for one year of full-time graduate study . FOREIGN EDUCATION: If you are using education completed… more
- Parexel (Harrisburg, PA)
- …authorities, including but not limited to: briefing documents, investigator brochures, study protocols, model informed consents, interim and final clinical study ... skills. + Scientific background essential; writing experience includes multiple clinical documents: study reports, study protocols, or CTD documents or similar.… more
- University of Pennsylvania (Philadelphia, PA)
- …associated site initiation documentation. Reporting to the Regulatory Affairs New Study & Continuing Review Manager, the Senior Regulatory Affairs Start-Up ... queries, and participate in the initiation of the new study , as well as communicate transition of the new..., as well as communicate transition of the new study to the applicable team Regulatory Affairs Specialist post-site… more
- PwC IT Services Co. (Pittsburgh, PA)
- …Minimum Years of Experience: 4 year(s) Preferred Fields of Study : Information Technology, Computer Systems Analysis, Management Information Systems. Preferred ... salary range for this position. **Education** _(if blank, degree and/or field of study not specified)_ Degrees/Field of Study required: Degrees/Field of Study… more
- Carnegie Mellon University (Pittsburgh, PA)
- …of bioprinted liver constructs in rodent and porcine models, including IND-enabling studies . The Research Scientist will play a central role in coordinating these ... studies , analyzing outcomes, and preparing regulatory documentation in collaboration...vitro efficacy testing and in vivo safety and functionality studies in rodent and porcinemodels. + Collaborate with regulatory… more