- 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
- Bank of America (Pennington, NJ)
- …focused on Special Investigations, Global Markets, or Global Wealth and Investment Management . In the investigative role, the Investigator conducts complex ... Global Financial Crimes Compliance (GFCC) Investigator - Brokerage Charlotte, North Carolina;New York, New...investigations while ensuring cases meet or exceed closure and quality metrics, reporting facts of the investigation to assist… more
- ManpowerGroup (Princeton, NJ)
- …and equipment related issues that occur during the Manufacturing process. The MS&T Specialist works closely with the Manufacturing and Quality teams to determine ... Pharma companies in the US, is looking for a ** Investigator , MS&T (Manufacturing Science and Technology)** which is located...is located at **Princeton NJ** . Looking for MS&T Specialist to provide technical support and expertise in gene/cell… more
- Bank of America (Pennington, NJ)
- …PowerPoint, Excel and Word; SharePoint, Webex, Mattermost **Skills:** + Coaching + Fraud Management + Quality Assurance + Regulatory Compliance + Investigation ... Senior Global Financial Crimes Investigator - Proficiency Coach Tampa, Florida;Plano, Texas; Charlotte,...providing coaching and inputs to investigators to improve case quality , ensure all cases are sufficiently investigated and findings… 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
- System One (Princeton, NJ)
- Title: Contracts Specialist Location: Remote Type of role: Full time contract Position Compensation: 85K - 90K The selected candidate will support successful ... Essential Functions - Project Support: + Reviews clinical trial protocols and develops investigator cost per patient budgets and site contracts for North America (US… more
- Penn Medicine (Plainsboro, NJ)
- …This employee will oversee the processes for study start-up and on-going study management from start to finish working closely with the CRU Regulatory coordinators ... source document tools, show vigilance in patient safety, protocol compliance and data quality . This employee must adhere to the requirements of the University of… 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