- job summary: We are seeking an experienced Regulatory Writer with a strong background in writing protocols, clinical study reports (CSRs), briefing books, informed consent forms (ICFs), and CTD Module 2 documents. This expertise is critical to the role. The successful candidate will play a key role in preparing high-quality regulatory documentation to support clinical and regulatory submissions, ensuring compliance with global regulatory requirements. Thijob summary: We are seeking an experienced Regulatory Writer with a strong background in writing protocols, clinical study reports (CSRs), briefing books, informed consent forms (ICFs), and CTD Module 2 documents. This expertise is critical to the role. The successful candidate will play a key role in preparing high-quality regulatory documentation to support clinical and regulatory submissions, ensuring compliance with global regulatory requirements. Thi
- job summary: We have a non-clinical Writing Opportunity immediately available. This will be remote, 20 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 regulatjob summary: We have a non-clinical Writing Opportunity immediately available. This will be remote, 20 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 regulat
- 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: Global Regulatory Operations Publishing | Undergrad Intern ~ Summer 2024 Are you a detail-oriented student eager to gain hands-on experience in Regulatory Operations and global health authority submissions? This internship offers a unique opportunity to contribute to the preparation and delivery of high-quality, timely, and compliant regulatory submissions in a fast-paced, cross-functional environment. As a Global Regulatory Publishing Underjob summary: Global Regulatory Operations Publishing | Undergrad Intern ~ Summer 2024 Are you a detail-oriented student eager to gain hands-on experience in Regulatory Operations and global health authority submissions? This internship offers a unique opportunity to contribute to the preparation and delivery of high-quality, timely, and compliant regulatory submissions in a fast-paced, cross-functional environment. As a Global Regulatory Publishing Under
- 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: Real-World Evidence & Biostatistics ~ Exclusive Summer Internship Opportunity We're looking for a highly motivated Master's or PhD student to join our Real-World Evidence (RWE) and Biostatistics research team for a Summer Internship. This role will focus on the application of Double Machine Learning in Causal Inference, providing exposure to real-world healthcare data and advanced statistical modeling techniques. The intern will work with crjob summary: Real-World Evidence & Biostatistics ~ Exclusive Summer Internship Opportunity We're looking for a highly motivated Master's or PhD student to join our Real-World Evidence (RWE) and Biostatistics research team for a Summer Internship. This role will focus on the application of Double Machine Learning in Causal Inference, providing exposure to real-world healthcare data and advanced statistical modeling techniques. The intern will work with cr
- 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: Job Description The Medical Writing Intern (MWI) assists with medical writing activities in support of the GCDO - Medical Writing & Transparency department. The MWI works closely with MW personnel to develop regulatory documents in support of company products. This individual will work to assigned timelines, communicate effectively to the responsible medical writer, and ensure their deliverables are completed according to appropriate qualityjob summary: Job Description The Medical Writing Intern (MWI) assists with medical writing activities in support of the GCDO - Medical Writing & Transparency department. The MWI works closely with MW personnel to develop regulatory documents in support of company products. This individual will work to assigned timelines, communicate effectively to the responsible medical writer, and ensure their deliverables are completed according to appropriate quality
- job summary: This person will be responsible for operational support of the MS&T and QC labs, including scheduling and overseeing maintenance of laboratory and process equipment. You will also be responsible for scheduling and tracking maintenance/repair activities within the CMMS. This is a 6-month contract requiring 100% on-site work from 8:30 AM to 4:00 PM. location: Philadelphia, Pennsylvania job type: Contract salary: $40 - 50 per hour wojob summary: This person will be responsible for operational support of the MS&T and QC labs, including scheduling and overseeing maintenance of laboratory and process equipment. You will also be responsible for scheduling and tracking maintenance/repair activities within the CMMS. This is a 6-month contract requiring 100% on-site work from 8:30 AM to 4:00 PM. location: Philadelphia, Pennsylvania job type: Contract salary: $40 - 50 per hour wo
