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. Thi
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. 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 regulat
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 regulat
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