Regulatory Submissions Coordinator (Senior/ Experienced)

About the role

They work hard, understand our high expectations, and rise to the challenge. In return they are rewarded with interesting projects, career advancement, and recognition and exposure to our international footprint. These are just a few reasons why talented individuals join the Medpace team. *Office based with hybrid work arrangements based on eligibility

What you'll do

• Perform required activities within the country that lead to activation of investigative sites in all phases of clinical trials; Prepare, review

What you need

• 4–7 yrs of experience
• Regulatory affairs
• Clinical research
• CRO
• Documentation
• Compliance
• Any graduate