Study Start-Up Coordinator - Regulatory Submissions

A clinical research organization is seeking a full-time Regulatory Submissions Coordinator in Cincinnati, Ohio. This role involves coordinating regulatory submissions, ensuring compliance, and communicating with research sites. Ideal candidates will have a Bachelor's degree in Life Sciences and at least 1-5 years of experience in study coordination or the pharmaceutical industry. Strong organizational and communication skills are essential. Join a team dedicated to advancing clinical trials with your expertise. #J-18808-Ljbffr