- 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