- 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: Job Description As we expand our business, we seek a motivated and skilled API Programming Intern to join our team and help develop advanced APIs that power our products and services location: Telecommute job type: Contract salary: $25 - 30 per hour work hours: 9 to 5 education: Bachelors responsibilities: Job Responsibilities Support EDC User Management and Site Administration activities.Understand how to build RESTful APjob summary: Job Description As we expand our business, we seek a motivated and skilled API Programming Intern to join our team and help develop advanced APIs that power our products and services location: Telecommute job type: Contract salary: $25 - 30 per hour work hours: 9 to 5 education: Bachelors responsibilities: Job Responsibilities Support EDC User Management and Site Administration activities.Understand how to build RESTful AP
- 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
- 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: Required: Must be currently enrolled in a Bachelor's degree program (Junior/Senior level)No industry experience requiredStrong verbal and written communication skillsBasic knowledge of Word, Excel, PowerPoint, and shared platforms (e.g., SharePoint, Box, Smartsheets) Preferred: Exposure to Good Clinical Practices (GCP) regulations and Standard Operating Procedures (SOPs)Understanding of clinical study phases and their role in clinicaljob summary: Required: Must be currently enrolled in a Bachelor's degree program (Junior/Senior level)No industry experience requiredStrong verbal and written communication skillsBasic knowledge of Word, Excel, PowerPoint, and shared platforms (e.g., SharePoint, Box, Smartsheets) Preferred: Exposure to Good Clinical Practices (GCP) regulations and Standard Operating Procedures (SOPs)Understanding of clinical study phases and their role in clinical
