- job summary: The CRA will be responsible for monitoring oversight, co-monitoring, and site management work to ensure that the CRAs working under the CRO(s) and the sites conducting the studies on behalf of Company, follow all applicable regulations, guidelines, and sponsor requirements. The CRA will work closely with study teams, investigators, and research sites to ensure the successful execution of clinical trials from start up through close out. Idealljob summary: The CRA will be responsible for monitoring oversight, co-monitoring, and site management work to ensure that the CRAs working under the CRO(s) and the sites conducting the studies on behalf of Company, follow all applicable regulations, guidelines, and sponsor requirements. The CRA will work closely with study teams, investigators, and research sites to ensure the successful execution of clinical trials from start up through close out. Ideall
- job summary: The Global Regulatory Operations Publishing Intern prepares and delivers high quality, timely, and compliant regulatory submissions to global health authorities. The Publishing Intern represents Global Regulatory Publishing in cross-functional project teams, provides regulatory submission support for products and contributes to regulatory initiatives location: Telecommute job type: Contract salary: $25 - 30 per hour work hours: 9job summary: The Global Regulatory Operations Publishing Intern prepares and delivers high quality, timely, and compliant regulatory submissions to global health authorities. The Publishing Intern represents Global Regulatory Publishing in cross-functional project teams, provides regulatory submission support for products and contributes to regulatory initiatives location: Telecommute job type: Contract salary: $25 - 30 per hour work hours: 9
- job summary: Job Description Intern, Global Patient and Site Engagement, will be a member of the GPSE team under GCDO. The Intern will work cross functionally across the portfolio supporting the vision to bring the patient and site voice into the clinical design and clinical trial working group teams, as well as study feasibility and global monitoring with activities related to site relationship management, strategic planning for new and ongoing studies,job summary: Job Description Intern, Global Patient and Site Engagement, will be a member of the GPSE team under GCDO. The Intern will work cross functionally across the portfolio supporting the vision to bring the patient and site voice into the clinical design and clinical trial working group teams, as well as study feasibility and global monitoring with activities related to site relationship management, strategic planning for new and ongoing studies,
- job summary: We have a CMC Regulatory Writing Opportunity immediately available. This will be remote, 10 hours per week, and offer a flexible schedule. Hourly Pay. location: Wayne, Pennsylvania job type: Contract salary: $90 - 100 per hour work hours: 9 to 5 education: Masters responsibilities: Work closely with client and internal and partner organization teams to lead development of strategies for organizing and preparing reguljob summary: We have a CMC Regulatory Writing Opportunity immediately available. This will be remote, 10 hours per week, and offer a flexible schedule. Hourly Pay. location: Wayne, Pennsylvania job type: Contract salary: $90 - 100 per hour work hours: 9 to 5 education: Masters responsibilities: Work closely with client and internal and partner organization teams to lead development of strategies for organizing and preparing regul
