Job Description
A leading clinical research organization is seeking a Study Start-up Associate Senior to oversee the preparation and submission of regulatory packages for clinical trials. This role involves coordinating timelines, customizing documents according to local regulations, and serving as a primary contact for study teams and sponsors. The ideal candidate will have over 6 years of experience in regulatory affairs, strong communication skills, and the ability to manage multiple priorities effectively. Join us to advance clinical research and impact patients' lives.
#J-18808-Ljbffr
#J-18808-Ljbffr
Apply for this Position
Ready to join Emmes Group? Click the button below to submit your application.
Submit Application