Medpace in Melbourne, Australia, is seeking an Entry level Regulatory Submissions Coordinator to join our Clinical Operations team. This office-based role supports study start-up and regulatory submissions under guidance.
You will work with global study teams, prepare and submit to TGA/Medsafe, and help ensure compliance with ICH-GCP and local regulations. A bachelor's degree and 1 year of CRO/pharma exposure are preferred.
Study Start-Up Regulatory Submissions Coordinator employer: Medpace
Medpace is an exceptional employer, offering a dynamic work environment in Melbourne that fosters professional growth and development within the clinical research field. With a strong focus on employee well-being, competitive compensation, and flexible working arrangements, Medpace supports its team members in achieving their career aspirations while contributing to meaningful advancements in medical therapeutics. Join a globally recognized leader in the CRO industry, where your expertise will be valued and your contributions will make a real impact.
