Medpace is seeking an entry-level Regulatory Submissions Coordinator for the Australia, Melbourne office to support study start-up activities within Clinical Operations.
You will handle regulatory submissions, coordinate with TGA/Medsafe, and assist global study teams while growing your regulatory expertise in a fast-paced CRO environment. The role offers exposure to international projects, hands-on document preparation, and opportunities for career development within a global CRO network.
Regulatory Submissions Coordinator – Study Start-Up in Melbourne employer: Medpace, Inc.
Medpace is an exceptional employer for those looking to launch their careers in clinical trial management, particularly in the vibrant city of Melbourne. With a strong focus on employee growth, Medpace offers comprehensive training programs, clear career advancement paths, and a collaborative work culture that fosters innovation and open communication. Employees benefit from competitive compensation, health and wellness programs, and a supportive environment that encourages professional development and meaningful contributions to advancing medical therapeutics.
