- 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: 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
