Associate Director Clinical Research, Country Feasibility Lead (Biopharmac)

Lead country feasibility activities for clinical trials in Korea, coordinate and evaluate feasibility for site selection, and serve as the first point of contact for feasibility questions. Manage and consolidate local site lists and feedback, support early recruitment modelling and scenario planning, and oversee feasibility-related materials and surveys. Collaborate with global teams to tailor local SQV materials, participate in handovers post-feasibility, and line-manage CRAs and CSAs. Requires strong knowledge of the Clinical Study Process and ICH-GCP guidelines, ability to deliver quality trials within budget and time, and experience working with remote collaborators. Proficiency in Korean and English is required to facilitate communication across local and global stakeholders.