Senior Regulatory and Start Up Specialist (Brazil)

Prepare and manage clinical trial submission documents for Competent Authorities and Ethics Committees. Act as a Subject Matter Expert for site start-up activities and mentor less-experienced staff. Maintain communication with key functions involved in country start-up and provide regular updates on submission statuses.

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.