Description
Precision Medicine Group is hiring its first Senior Regulatory and Start Up Specialist in Argentina to lead clinical trial site activation and regulatory submissions. The role covers initial and subsequent submissions to competent authorities and ethics committees, informed-consent and essential-document review, study start-up planning, site collaboration, budget and contract support, translation coordination, audit readiness, and mentoring of less-experienced staff. The position requires a bachelor’s degree in life sciences or a related field, or an RN or equivalent combination, plus at least 3.5 years of regulatory or site start-up experience in a CRO or pharmaceutical/biotech industry. The role is marked remote and may require occasional travel.
