Prepare, review, and file clinical trial applications to domestic and international regulatory agencies;
Ensure submissions comply with applicable regulations and guidance documents;
Advise sponsors on changing regulations and compliance requirements; and
Track submissions and ensure timely filing of documents.
Bachelor's degree in life sciences;
Excellent organization and communication skills;
Knowledge of Microsoft® Office; and
Hands-on experience preparing, reviewing, and submitting regulatory documentation;
At least one year of work experience as a Regulatory Submissions Coordinator ;
Fluency in English and Hungarian language.
Finding work that is challenging, where you are given the tools and training to succeed, where you are rewarded and are provided opportunities to grow professionally are just a few reasons talented individuals join the Medpace team.
WHAT TO EXPECT NEXT
We look forward to receiving your application. A member of our recruitment team will review your qualifications. If interested, you will be contacted for an interview.