Regulatory and Start Up Specialist

The Regulatory and Start Up Specialist at Precision for Medicine supports regulatory activities and site start-up efforts to ensure timely site activation and compliance with international and local clinical trial regulations. The role coordinates submissions to Competent Authorities and Ethics Committees, maintains project trackers and regulatory intelligence, and partners with clinical teams and sites. This position contributes to document management, translation coordination, and audit readiness to enable the conduct of clinical trials in oncology and rare diseases.