- 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
- 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: Responsibilities Technical Lead aligned to modernization/data service strategy Qualifications modernization/data service strategy location: Malvern, Pennsylvania job type: Contract salary: $56.73 - 61.73 per hour work hours: 8am to 5pm education: Bachelors responsibilities: Responsibilities Technical Lead aligned to modernization/data service strategy Qualifications modernization/data service strategy qualifijob summary: Responsibilities Technical Lead aligned to modernization/data service strategy Qualifications modernization/data service strategy location: Malvern, Pennsylvania job type: Contract salary: $56.73 - 61.73 per hour work hours: 8am to 5pm education: Bachelors responsibilities: Responsibilities Technical Lead aligned to modernization/data service strategy Qualifications modernization/data service strategy qualifi
- 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
