- 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
- 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
- ICON Clinical Research (Blue Bell, PA)
- …Recruitment and Screening Services. 2. *Conduct of studies * To act as Co- Investigator for studies, actively supporting the Principal Investigator in the ... a rotational basis. 4. *Study protocols/reports * Assist project management in the leadership of studies. * To meet...done with the knowledge and support of the Principal Investigator . * To attend Research Ethics Committee meetings when… 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