- job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtijob summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longti
- job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtijob summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longti
- 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
- job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtijob summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longti
- 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: 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
- job summary: Real-World Evidence & Biostatistics ~ Exclusive Summer Internship Opportunity We're looking for a highly motivated 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 cross-functionjob summary: Real-World Evidence & Biostatistics ~ Exclusive Summer Internship Opportunity We're looking for a highly motivated 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 cross-function
- 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: 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: 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
