- Devereux Advanced Behavioral Health (Berwyn, PA)
- **Description** We are looking for a Quality Management Specialist to conduct investigations involving individuals with intellectual and developmental ... safety and to decrease risk + Other duties as required As a quality Management investagator you will monitor compliance with all regulatory and funding agencies.… more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Regulatory Affairs Specialist C Job Profile Title Clinical Research Regulatory Specialist C Job ... independently with minimal supervision on complex protocols. The Regulatory Affairs Specialist C reviews and creates core documents (protocols, Informed Consents, … more
- University of Pennsylvania (Philadelphia, PA)
- …and wellness programs and resources, and much more. Posted Job Title Veeva Quality Assurance Specialist (Abramson Cancer Center) Job Profile Title Clinical ... Regulatory Affairs Office seeks a full-time Regulatory Affairs Veeva Quality Assurance Specialist to participate in the...the review and migration of Phase I-V clinical trial investigator site files to the Veeva SiteVault platform. Reporting… more
- Merck (West Point, PA)
- …+ Interacts with key partner organizations such as clinical development, regulatory, quality and other supply chain areas to address clinical supply related topics. ... preparation and presentation of the clinical supplies information at Investigator Meetings for assigned protocols. + Support the collection...required. + At least 5 yearsof experience in project management + At least 5 years of experience in… more
- University of Pennsylvania (Philadelphia, PA)
- …oversee the start-to-end processes for study start-up and ongoing study management . This includes assisting with study feasibility and selection, prioritization of ... source document tools, show vigilance in patient safety, protocol compliance and data quality . Adhere to the requirements of the University of Pennsylvania, GCP, FDA… more
- CSL Behring (King Of Prussia, PA)
- …and marketing in developing strategies and implementing tactics. + Ensure the quality and relevance of all Medical Affairs led research ( Investigator -initiated ... Review Committee (PRC) oversight of the PharmD Medical Information Specialist (s). + Partner and collaborate with the global...& Pharmacovigilance (GCSP) and will serve on the Safety Management team for key US products. **Main Responsibilities and… more
- University of Pennsylvania (Philadelphia, PA)
- …studies. This position is responsible for study coordination for investigator -initiated studies, multi-center research studies, and patient-oriented clinical and ... of ACE-WS and show vigilance in patient safety, protocol compliance, and data quality . It requires adherence to all University of Pennsylvania, IRB, and FDA… more
- University of Pennsylvania (Philadelphia, PA)
- …oversee the start-to-end processes for study start-up and ongoing study management . This includes assisting with study feasibility and selection, working closely ... source document tools, show vigilance in patient safety, protocol compliance and data quality . Adhere to the requirements of the University of Pennsylvania, GCP, FDA… more
- TD Bank (Mount Laurel, NJ)
- …for minimizing losses to customers and the Bank and contributing to the management of adverse impacts and reputational risks as part of the resolution and ... In the check claims department, the agent works the investigator process. They will review documents, speak with Customers,...and the Bank against fraud + Acts as deep specialist /expert within defined area and be a key resource… more