Responsibilities : - Preparation of regulatory documents, CTA packages, and submissions in assigned countries to ensure high quality standards - Coordination of regulatory timelines and deadlines for all assigned projects planned for CTIS submissions. Includes oversight
Description Principal / Senior Medical Writer - with proven strong clinical document writing experience Principal / Senior Medical Writer - with proven strong clinical document writing experience Syneos Health® is a leading fully-integrated life sciences services
The Regulatory Affairs Associate will support the preparation, tracking, and coordination of Ethics Committee (EC) and Regulatory Authority (RA) submissions. Under supervision, the Associate will assist the Regulatory Affairs team in ensuring that clinical trial submissions