Found Description
Study Start Up Associate II (Regulatory Submissions) – Chile – Hybrid Scheme
Senior Study Start Up Associate will support the Study Start Up Team Lead in planning country and site distribution and executing SSU activities across assigned countries.
Responsibilities
- Conduct feasibility assessments, site identification, and site contract negotiation.
- Provide country‑specific SSU expertise to Study Start Up team leads and project teams.
- Prepare and coordinate submissions to regulatory, ethics, and other bodies.
- Develop, finalize, and review Master and Country Specific Subject Information Sheets/Informed Consent Forms.
Qualifications
- Bachelor’s degree or equivalent and/or relevant experience in a medical or science background.
- Minimum of 2 years of experience or understanding of clinical study start‑up requirements and activities.
- Strong knowledge of regulatory requirements and guid...
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