Sarah Bess Email and Phone Number

With over eight years of experience in clinical research, I am a Senior Regulatory Submissions Coordinator at Medpace, a leading global clinical research organization. In my current role, I oversee the preparation and submission of regulatory documents for various clinical trials, ensuring compliance with Good Clinical Practice (GCP) and other relevant guidelines. I work with a diverse and collaborative team of regulatory professionals, project managers, sponsors, and investigators to facilitate the timely and successful completion of clinical studies. I have also contributed to the development and improvement of regulatory processes and procedures within the organization. My core competencies include regulatory submissions, clinical research, GCP, project management, communication, and problem-solving. I am motivated to accelerate the global development of safe and effective medical therapeutics, and I strive to bring my expertise, skills, and enthusiasm to every project I work on.