- 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 Clinical Research Quality Specialist C (Office of Clinical Research) Job Profile Title Clinical ... Research Quality Specialist C Job Description Summary The...compliance activities for sponsored IND clinical research trials and Investigator initiated trials to verify human subjects are safe,… 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
- ThermoFisher Scientific (Wilmington, DE)
- …digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities ... define and develop clinical programs, minimize delays, and execute high- quality , cost-efficient clinical studies. This position requires overnight travel either… 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
- 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