Regulatory Submissions-Start Up & Contract Specialist (dual role)
Core
Prepare, review, and file clinical trial applications to regulatory authorities and Ethics committees in Latvia; draft, negotiate, and finalize legal agreements for clinical studies.
Role type
Regulatory Submissions Coordinator & Contract Specialist
Builds
Clinical trial submissions and study agreements for biotechnology, pharmaceutical, and medical device companies
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 or Law degree, CRO/Pharma experience, independent work style
Technologies
Clinical Trial Management System, Microsoft Office
