Lead statistical planning and execution for clinical studies: author SAPs, review datasets and TLFs, oversee QC and database activities, mentor junior staff, manage timelines and budgets, and communicate with clients.

Lead development and management of complex investigator grant estimates and site contracts for clinical trials. Create templates, processes, and training; provide legal, operational and financial contracting support; ensure sponsor and regulatory compliance; maintain contracting systems and CTMS; report metrics; mentor colleagues and liaise with sponsors and stakeholders to deliver project scope and timelines.