Study Startup Specialist II/I

Take your career to the next level and lead challenging study activation process on a country/regional level. You will support clinical research teams and ensure PSI projects start smoothly and on time.  Office Base: Shanghai or Beijing You will:   • Maintains study-specific and corporate startup tracking systems. • Facilitates site budgets and contract negotiations. • Supports site regulatory document collection. • Under supervision, may prepare initial submission dossiers to competent authorities, ethics committees, and/or site submission dossiers (as applicable). • Communicates with the project team and investigational sites throughout the study startup phase. • Develops site specific startup timelines and enrollment projections and is responsible for meeting the site activation milestones. • May review study specific translations. • Supervises Trial Master File (TMF) maintenance throughout the study startup phase.   • Bachelor's degree of Medical, Pharmaceutical or any Life Sciences related major • At least 2 years site startup experience • Well-developed communication and organizational skills • Ability to negotiate and build relationships at all levels • Leadership, mentoring, and organizational skills • English and Japanese skills (High Business level to Fluent) Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with a rapid growing company, that puts its people first!