General Counsel

• Overview: The Assistant General Counsel - Privacy & Regulatory will work closely with members of the Legal and Compliance Teams in the drafting, implementing, and overseeing the organization’s global privacy, regulatory, and legal compliance programs, enabling adherence to applicable laws and regulations (e.g., HIPAA, CCPA, GDPR) and industry standards (CLIA, NYS).
• Serve as subject matter expert and internal escalation point for privacy and data protection issues in contracting, sales and marketing, business development and operations.
• Ensure the organization has appropriate privacy contract provisions, including DPAs, Business Associate Agreements, Standard Contractual Clauses and Transfer Impact Assessments, if and as required.
• Monitor developments in data protection, regulatory, and privacy laws applicable to advanced diagnostics, and develop and lead cross functional project teams to support company compliance.
• Provide practical legal advice on data driven projects while anticipating and navigating regulatory and privacy considerations, including data sharing and analytics, mobile applications, and use of artificial intelligence.
• Participate in the review of customer-facing materials for alignment with applicable data protection and privacy policies, laws, and regulations.
• Oversee and provide legal advice on privacy incident and breach response program.
• Provide legal advice on the use of technology within the organization (e.g. enterprise digital marketing, websites).
• Partner with Information Security, Governance/Risk/Compliance (GRC), and Government Affairs on diagnostics regulatory oversight (FDA/CLIA etc.), privacy and cyber related policy/regulation impacting the company.
• Create and/or assist with privacy operations management, including, where applicable, DSARs, data mapping, data inventory, records of processing activities, DPIAs and PIAs.
• Provide legal advice to support compliance with HIPAA, GDPR, global privacy regulation, and state genetic testing, data breach notification, regulatory and privacy laws.
• Provide support for human subject research, IRB protocol, and informed consent review in compliance with the Common Rule and Clinical Trial Regulations.
• Provide privacy and regulatory advice in research and commercialization collaborations and M&A transactions and integrations.
• Assist in special projects and other duties as assigned.
• Physical Requirements: sedentary work or exerting up to 10 pounds of force occasionally; stationary positioning, moving, communicating, and observing.

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