- Devereux Advanced Behavioral Health (Berwyn, PA)
- …YES, then consider joining our Devereux Advanced Behavioral Health team! **Being a Quality Management Specialist at Devereux has its Advantages** You ... **Description** Are you interested Quality Management ? Do you enjoy making sure things run smoothly? If you answered… 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
- University of Pennsylvania (Philadelphia, PA)
- …The specialist will be closely working with the Principal Investigator and other lab members on translational science publication-generating projects but is ... The specialist will be closely working with the Principal Investigator and other lab members on translational science publication-generating projects but is… 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