Associate Director, Study Site Engagement

Requirements

• By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use .
• I further attest that all information I submit in my employment application is true to the best of my knowledge.
• The Associate Director, Study Site En gagement establishes communication with regional/country Medical Affairs (MA), provides up dates on study/site status, and establishes site engagement study specific strategies.
• Associate Director, Study Site Engagement supports study teams with trial operations from Feasi bility through CSR within the assigned region or countries across Takeda therapeutic areas.
• The Associate Director, Study Site Engagement supports country and site identification, feasibility, site selection, study recruit ment strategies, and mitigates barriers at the direction of Clinical Programs.
• The Associate Director, Study Site Engagement supports Takeda study teams as part of their day to-day responsibilities and may act as an SSE-Program Lead (SSE-PL) and/or SSE-Study Lead (SSE-SL).
• Attends Pre-Study Visit (PSV) as requested or agreed upon with the SSE-SL.
• Helps to follow up with country MA, local Clinical Operations team and keep track of country and site selection activities.