Working across assigned products and therapeutic areas, the Director partners with Medical Affairs operational counterparts and Global Development/Post Approval Delivery Unit teams to translate evidence-generation strategy into the compliant clinical and operational implementation of Company Sponsored Studies (CSS), Investigator Initiated Studies (IIS), Collaborative Studies, and other post-marketing research conducted through insourced, outsourced, or matrixed organizations. Budgeting, Clinical Trials, Clinical Trials Operations, Coaching, Compliance Management, Contract Management, Developing Others, Execution Focus, Fact-Based Decision Making, Give Feedback, Inclusive Leadership, Laboratory Operations, Leadership, Process Improvements, Project Integration Management, Research and Development, Research Ethics, Technical Credibility