Regulatory Submissions-Start Up & Contract Specialist (dual role)
Core
Prepare, review, and file clinical trial applications to regulatory authorities and Ethics committees in Estonia; draft, review, and negotiate legal agreements for clinical studies.
Role type
Regulatory Submissions & Contract Specialist (dual role)
Builds
Clinical trial submissions and study agreements for biotechnology, pharmaceutical, and medical device clients
Domain
Clinical Research / Regulatory Affairs / Contract Management
Required skills
Regulatory documentation preparation, contract negotiation, risk assessment, Clinical Trial Management System (CTMS) maintenance, local regulatory guidelines knowledge, Microsoft Office
Preferred skills
Life Sciences/Business/Law degree background, CRO/Pharma site experience, independent work style
Technologies
Clinical Trial Management System (CTMS), Microsoft Office
