Regulatory Submissions Specialist – Study Start-Up (London)

Medpace, Inc. is seeking a Regulatory Submissions Coordinator to join the Clinical Operations team in London. This office-based role is essential in managing clinical trials, requiring a Bachelor’s degree in Life Sciences and experience in regulatory documentation. Key responsibilities include preparing and reviewing clinical trial applications, ensuring compliance with regulations, and advising team members. Benefits include a flexible work environment, competitive compensation, and structured career paths for growth.#J-18808-Ljbffr…