Senior Regulatory and Start Up Specialist (Argentina)

Prepare and submit Clinical Trial Application Forms and submission dossiers to Competent Authorities and Ethics Committees. Maintain communication with key functions involved in country start-up and provide regular updates on submission statuses. Act as a Subject Matter Expert for site start-up activities and mentor less-experienced staff.

Bachelor's degree in life sciences or related field, or Registered Nurse (RN). 3.5 years or more as a Regulatory or Start Up specialist in a CRO or pharmaceutical/biotech industry. Proficient in English communication, both verbal and written.