Initiating, drafting, redlining, and negotiating moderately complex clinical related contracts (Non-Disclosure Agreements, Master Clinical Trial Agreements, Scope of Work, Trial Budgets, Trial Purchase Agreements) based on substantial knowledge policy and regulations governing Clinical Trials and Edwards Policy. Identifying risk associated with project timelines set by project teams, impacting team’s deliverables and timelines, and key stakeholders’ workload (e.g., Legal Compliance, legal contracts, legal privacy, and risk management) based on revised timelines.