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medpace
Regulatory Submissions-Start Up & Contract Specialist
Remote · Estonia · Full time · Entry level
About the role
This dual role involves regulatory submissions and contract negotiations supporting clinical projects. You will gain hands-on experience and develop your clinical research career.
What you’ll do
• Prepare and file clinical trial applications in Estonia. • Submit responses to queries and amendments. • Ensure compliance with regulations and guidance. • Draft, review, negotiate, and finalize agreements. • Coordinate site startup activities with internal departments.
What you’ll bring
• Bachelor's degree in Life Sciences, Business or Law. • Experience with regulatory documentation and submissions. • Knowledge of local regulatory guidelines and legislation. • Fluency in Estonian and English. • Excellent organizational and communication skills.
Life at medpace
Medpace offers continuous learning, career advancement, competitive compensation, health and wellness benefits, and a collaborative culture with accessible leadership.
About medpace
Medpace is a global clinical contract research organization providing phase I-IV clinical development services to biotech, pharmaceutical, and medical device industries.