Director/Senior Director, Contracts and Transactions

Posted 5 Days Ago
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Vancouver, BC, CAN
In-Office
170K-230K Annually
Senior level
Biotech
The Role
Lead contract drafting, review, negotiation, and lifecycle management for research, development, software licensing, and general business agreements. Advise senior leaders and internal teams on contractual risks, commitments, and negotiation priorities. Support complex technology licenses and biopharma collaborations while maintaining the contract management system. Partner with Business Development, R&D, Procurement, Finance, and executive leadership to provide practical, business-oriented legal guidance.
Summary Generated by Built In
Company Profile
Genevant is a technology-focused nucleic acid delivery company with world class platforms, the industry’s most robust and expansive lipid nanoparticle (LNP) patent portfolio, and decades of experience and expertise in nucleic acid drug delivery and development.   We have laboratories and a key office based in beautiful Vancouver, British Columbia.

We leverage our innovative delivery systems and related technologies to bring new medicines to patients who need them. We do this by selectively collaborating with leading pharma and biotech companies and fostering a culture of innovation that allows us to maintain our leadership position in the space. If you find that inspiring, we want to work with you!
Position Summary
Genevant has an opportunity for an experienced, practical and commercially minded Director/Senior Director, Contracts and Transactions, to join our Legal team. Reporting to the Chief Legal Officer (CLO), this role will provide legal and transactional support across the organization, with a particular focus on research and development-related contracts and technology licenses and collaborations. The ideal candidate will thrive working independently to manage and execute on the day-to-day contracting required to keep a biopharma business moving, with the ability to grow into a leadership role for complex business negotiations.
The successful candidate will work closely with the CLO, senior leadership, Business Development, R&D, Procurement, Finance, and other functional leaders and is comfortable participating in and guiding executive level business/legal discussions. This is a hybrid position based in Vancouver, B.C.
Responsibilities:
  • Draft, review, negotiate and otherwise manage the contracting process for a wide variety of contracts, including research and development-related agreements, software licenses and other G&A agreements, to align with Genevant’s objectives.
  • Support the CLO and other members of senior leadership and grow into a leadership role in the negotiation and preparation of complex technology licenses and collaborations.
  • Maintain a well functioning contract management system.
  • Support contract lifecycle management, including tracking agreements, renewals, amendments, extension and key dates.
  • Act as a trusted legal business partner who provides practical, business-oriented legal advice and explains complex legal issues in clear, understandable terms.
  • Help internal teams understand contractual commitments, risks, and negotiation priorities.
  • Manage other legal-related responsibilities as assigned by the CLO.

Requirements, Knowledge, skills, and abilities:
  • Juris Doctor from a recognized law school.
  • 2-6 years of relevant experience in-house / law firm experience in a contracts or general corporate role, preferably within the life sciences industry.
  • Experience with complex pharma collaborations is a plus.
  • Strong communication and executive presence, with credibility at the senior leadership level.
  • Proven experience in contract negotiation and management, with the ability to lead the process independently end-to-end.
  • Strong problem-solving and analytical skills with the ability to collaborate effectively in fast-paced, dynamic environments.
  • Strong business acumen with sound judgment in integrating legal advice with business objectives.
  • Licensed to practice law in British Columbia and in good standing with the Law Society of BC.
  • Need to interact with colleagues in Eastern (3-hour time difference) and Central European time zones (9-hour time difference) may require worktime flexibility.
  • Occasional travel may be required. 

Benefits & Compensation
We’ve worked to create an environment at Genevant that makes our people feel empowered, supported and appreciated so they can focus on doing incredible work that can change the future. To that end, we offer competitive salaries, performance bonus opportunity, as well as a generous benefits package including health, dental, vision, wellness, short- & long-term disability, accident death & dismemberment, and life insurance programs; company match towards retirement savings and ample time off through our flexible PTO and annual company shutdown!
The Canadian base salary range for this position is CAD$170,000 – 230,000 excluding performance bonus and benefits. The base salary is determined by various factors including, but not limited to, education, qualifications, experience, and internal equity. The salary offered may be higher or lower than the posted range, depending on the candidate’s qualifications and other factors.
 

Skills Required

  • Juris Doctor degree from a recognized law school
  • 2-6 years of relevant in-house or law firm experience in contracts or general corporate law
  • Experience with contract negotiation and management, including independently leading processes end-to-end
  • Licensed to practice law in British Columbia and in good standing with the Law Society of British Columbia
  • Strong communication, executive presence, problem-solving, analytical, collaboration, and business judgment skills
  • Life sciences industry experience
  • Experience with complex pharmaceutical collaborations
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The Company
HQ: Vancouver, British Columbia
54 Employees

What We Do

Genevant is a technology-focused nucleic acid delivery company with world-class platforms, the industry’s most robust and expansive lipid nanoparticle (LNP) patent estate and decades of expertise in nucleic acid drug development. We leverage our world-class delivery systems and related technologies to bring new medicines to patients who need them. We do this by selectively collaborating with leading pharma and biotech companies and fostering a culture of innovation that allows us to maintain our leadership position in the space. • Best-in-class LNP + next generation ligand conjugate technologies • First and only FDA-approved siRNA-LNP utilizes Genevant technology • Nucleic acid payload design expertise • Several hundred patents worldwide • LNP technology evaluated in more than a dozen clinical programs, representing hundreds of subjects and patients • An established leader in delivery to the liver, now focusing capabilities on other tissues and cell types • Experienced team with deep technical expertise and a track record of innovation and creative corporate partnering

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