Specialized in-house and law firm experience focused on providing essential legal risk mitigation guidance that effectively preserves underlying business objectives.Drafted and negotiated joint development agreements, material transfer agreements, clinical study supply agreements, laboratory services agreements, SaaS agreements, cooperative research and development agreements, PBM agreements, medical device regulatory filings, clinical trial agreements, MDR compliance agreements, investigator initiated study agreements, GPO agreements, purchase agreements, complex software license agreements, patient recruitment and consulting agreements, professional advisor agreements, cyber security compliance agreements, MSAs, vendor and reseller agreements, OEM agreements, non-disclosure agreements, third-party agreements, real estate leases, acquisitions and divestitures, right of way agreements and government teaming and procurement agreements.Licensed, managed and protected intellectual property portfolios.Provided in-depth analysis of state and federal governmental regulations and legislation and have drafted and implemented policies to ensure clients’ regulatory compliance, including HIPAA, GDPR, CCPA, HITECH, FERC, FCRA, FMLA, FISMA, FDA, FCC, SOX, FTC, SEC, EPA and ERISA regulations.Collaborated with internal teams formulating business development strategies resulting in strong consistent growth to a variety of clients ranging from startups to Fortune 100 companies.Developed and presented risk mitigation, employee conduct best practices, contractual pitfalls and other employee training seminars.Developed and implemented digital health program for a multi-regional healthcare system.