Associate Corporate Counsel

C4 Therapeutics Inc • Watertown, MA

2d

About The Position

As our Associate Corporate Counsel, you will assume a key role within the Legal and Business Operations of C4T as we rapidly advance towards commercialization. Partnering closely with our Clinical Development team, you will work cross-functionally to advise your internal clients, drafting and negotiating contracts with external parties, review policies, and communications and filings. In partnership with our SVP, General Counsel, you will assist with the development of our reporting to the Securities and Exchange Commission, preparing a wide variety of reports, ensuring compliance with regulations and listing standards. Your strong track record in legal drafting, oral and written communication, negotiation and business partnering skillset demonstrated in the life science industry will be key as we go through this exciting phase of our organizational growth and deliver on the promise of targeted protein degradation to patients.

Requirements

• A Juris Doctor degree from an accredited law school, and admission to a state bar association in the United States, with a minimum of five years of post-graduate legal experience, including
• Significant experience drafting corporate and commercial agreements, including but not limited to clinical trial site agreements, CRO agreements, manufacturing and other supply chain agreements and licensing agreements
• Proven track record of effectively partnering with business teams throughout the transactional and negotiation process from beginning-to-end, in order to provide practical, timely, and solution-oriented advice, and to efficiently bring contracts to a favorable close.
• Capable of appropriately triaging multiple workflows simultaneously, setting clear priorities and expectations with clients and external parties, and efficiently delivering results in a pragmatic and risk-balanced manner, ensuring a strong level of detail-orientation while still delivering results on time.
• Ability to develop and maintain strong business relationships across the company and contribute to cross-functional or departmental projects, including demonstrated ability to identify potential legal issues and propose solutions to address business requirements while appropriately mitigating risk

Nice To Haves

• Experience working in a life science company either at commercial stage, or preparing for first commercial launch.

Responsibilities

• Serve as a business partner to and support the Clinical Development organization, including the clinical operations, regulatory and CMC teams
• Draft and negotiate a variety of contracts and agreements, including but not limited to, clinical trial site agreements, as well as licensing agreements, MSAs, SOWs and change orders with CROs, manufacturing and other supply chain vendors, service providers, etc.
• Support all aspects of clinical trial start up and maintenance, including review of patient informed consent forms, HIPAA authorizations and other trial related materials
• Interpret laws, rulings, and regulations to advise SVP, General Counsel and Clinical Development teams on legal and regulatory compliance matters to effectively understand and manage risk.
• Advise team on considerations as we approach commercialization, including providing guidance as we develop marketing and promotional materials, ensuring compliance with company policies, industry standards, and applicable laws and regulations.
• Partner closely with other Legal, IP, Privacy, and Compliance colleagues on special projects and committees as assigned.
• Help to direct the work of external legal counsel to ensure appropriate service and quality levels and to contain costs.
• Join the Legal/Contracts team in its efforts to effectively manage the delivery of legal services.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree
• Number of Employees: 11-50 employees