Senior Director, General Counsel

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Senior Director, General Counsel

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Work Location: Tevogen Corporate HQ, Warren, NJ
Reports to: Chief Executive Officer
Position: Full-time, Exempt

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Essential Duties and Responsibilities:

As a member of the leadership team, you will serve as the principal legal officer and lead the general legal function and compliance function at Tevogen Bio. Your main responsibilities will involve providing oversight across
departments, including finance and R&D departments. In addition, your regulatory experience will be leveraged to advise on the evolving regulatory and governance compliance environment.

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• Advise and counsel on general securities law, NYSE and NASDAQ matters, and general corporate governance matters.
• Collaborate with internal stakeholders on SEC filings, such as 10-Ks, 10-Qs, 8-Ks, and proxy statements.
• Assist with communications related to trading windows and equity related communications.
• Assist with the preparation of materials to be provided to the Board of Directors and its committees as needed.
• Draft and review amendments to governance documents, corporate policies and procedures, and Board committee charters as needed.
• Provide leadership on cross-functional teams, identify legal issues, and provide legal options/analysis of possible legal solutions.
• Proactively address the rapidly evolving regulatory and governance compliance environment including changes in laws and regulations, regulatory focus areas, and industry best practices.
• Draft, negotiate, and review various research and development agreements, including but not limited to, clinical trial agreements, informed consent documents, clinical supply agreements, quality agreements, investigator-initiated study agreements, contract research organization (CRO) agreements, and confidentiality agreements.
• Be responsible for advising clients on U.S. and ex-U.S. regulatory matters and compliance with laws, regulations, rules, guidance, industry standards, and company policies and procedures that arise through out the product life cycle, including in the areas of product development, regulatory submissions and strategy, social media, data, research and development, quality system compliance, etc.
• Work with colleagues to develop appropriate and compliant strategies for interacting with healthcare providers, payors, government officials, and other stakeholders.

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  Full Job Description

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