The Company:
With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.
The Role:
Reporting to the Deputy General Counsel, Corporate and Securities, the Counsel, Legal Affairs will be a hands-on, innovative, and collaborative attorney with experience in the biotechnology or pharmaceutical industry to act as our Counsel, Legal Affairs.
The legal team member will be a will partner with the Deputy General Counsel and other team members on a broad range of matters to provide high quality legal, compliance, and contracting advice to help advance Nuvalent's business strategy, while exercising discretion, professionalism and solid judgment. This exciting position will be a key member of our legal team with the opportunity to make an important impact on our company while ensuring a cohesive, collaborative, inclusive, and fun workplace experience.
Responsibilities:
- Independently support precommercial and commercial legal needs, including drafting, negotiating, and reviewing a broad range of commercial contracts, including commercial supply, patient hub services, product purchase, speaker, market access and commercial vendor agreements.
- Actively and effectively provide clear legal advice to internal stakeholders across key business functions, including support for commercial, medical and pipeline initiatives.
- Assist Deputy General Counsel in managing public securities legal and compliance-related matters, collaborating with internal stakeholders on SEC filings, such as 10-Ks and 10-Qs, 8-Ks and proxy statement, while leading others, including Section 16 filings
- Assist Deputy General Counsel and CLO with corporate governance matters, including drafting and reviewing minutes, maintaining committee charters and other key governance documents, and developing quarterly meeting agendas
- Stay current with evolving legal guidance and pharmaceutical, regulatory and policy initiatives, and partner with key stakeholders to develop, implement and maintain policies and procedures to ensure compliance in a way that advance’s the company’s strategy while protecting its integrity and reputation.
- Act as an advisor on legal issues involving the organization’s governmental, privacy and regulatory compliance
- Drive strong company culture as we grow and evolve
Competencies:
- Strong written and verbal communication skills and demonstrated ability to work both independently and collaboratively with people at different levels
- Ability to distill complexity and to communicate decisively with sound judgment
- Intellectual curiosity and an interest in working on a broad variety of legal matters
- Excellent organizational skills, attention to detail, and ability to multi-task and handle multiple projects simultaneously in a fast-paced, deadline-driven, cross-functional environment
- High-energy professional with demonstrated self-confidence, high integrity, and ability to maintain a high level of confidentiality and discretion in handling sensitive legal matters
- Desire to be a key part of a high growth, precommercial stage pharmaceutical company
Qualifications:
- 4+ years legal experience with a publicly traded biotechnology or pharmaceutical company and or a law firm advising internal stakeholders or clients on commercial contracting, public company reporting and compliance matters
- Prior commercial experience is required; experience advising a company through its initial commercial launch preferred.
- Broad, legal counsel experience in an emerging, publicly traded company environment is a plus.
- Juris Doctorate from an accredited law school and member of at least one U.S. state bar required
- Experience with drafting and negotiating a broad range of contracts specific to precommercial and commercial life sciences companies
- Strong knowledge of laws relevant to precommercial and commercial stage public companies focused on the discovery, development and commercialization of biopharmaceutical products, including but not limited to relevant FDA, securities, employment and other laws.
- Understanding of pharmaceutical regulatory and compliance environment and working knowledge of general corporate matters
Nuvalent provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.
Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.
Please be advised that all legitimate correspondence from a Nuvalent employee will come from "@nuvalent.com" email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “[email protected]” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person.
If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.
What We Do
Nuvalent is creating precisely targeted therapies for patients with cancer designed to overcome the limitations of existing therapies for clinically proven kinase targets. Leveraging deep expertise in structure-based design, Nuvalent develops innovative small molecules with exquisite target selectivity to overcome resistance, minimize adverse events, and drive more durable responses. Nuvalent is advancing a robust pipeline with parallel lead programs in ROS1-positive and ALK-positive NSCLC, along with multiple discovery-stage research programs. To learn more, visit www.nuvalent.com.
