Job Description Summary The Study Start Up (SSU) Associate function is to support the SSU Manager with all SSU‑related activities in collaboration with other clinical research stakeholders and to serve as a contact for local/global SSU process improvements. Key Responsibilities Coordinates and assists with all start‑up activities prior to site activation, including but not limited to: Submission of required documents to ethics committees, regulatory authorities, sites and sponsor. Submission of the clinical study agreement for review, as needed. Contribution to/coordination of site Informed Consent Form (ICF) localization and guidance in line with regulatory / health authority requirements. Contribution to localize global Informed Consent Form (ICF) with country requirements. Understanding and dissemination of information related to Ethics Committee, meeting dates
