Director, Legal
Company: Dr. Phillips Center
Location: Boston
Posted on: November 11, 2024
Job Description:
Who We Are:
Xenon Pharmaceuticals (NASDAQ:XENE ) is a neuroscience-focused
biopharmaceutical company committed to discovering, developing, and
commercializing innovative therapeutics to improve the lives of
people living with neurological and psychiatric disorders. We are
looking for great people who thrive in a respectful, collaborative,
inclusive, and productive culture to join the Xenon team. What We
Do:
We are advancing an exciting product pipeline to address
indications with high unmet medical need, including epilepsy and
depression. Our flagship azetukalner program represents the most
advanced potassium channel modulator in clinical development for
multiple indications. Building upon the positive results and
compelling data from our Phase 2b "X-TOLE" study in adult patients
with focal epilepsy, our Phase 3 epilepsy program includes multiple
clinical trials evaluating azetukalner in patients with focal onset
seizures and primary generalized tonic-clonic seizures. In 2024, we
are planning to initiate a Phase 3 azetukalner program in major
depressive disorder, based on topline data from our Phase 2
"X-NOVA" clinical trial. In addition, we are proud of the
leading-edge science coming out of our discovery labs, including
early-stage research programs that leverage our extensive ion
channel expertise and drug discovery capabilities to identify
validated drug targets and develop new product candidates. Backed
by a strong balance sheet to support our growth plans, we continue
to build a fully integrated, premier neuroscience company with
strong discovery, clinical development, corporate, and commercial
operations.
About the Role:
We are seeking a Director, Legal, to join our team as we expand our
Legal Affairs team. The ideal candidate is an experienced leader
with contracts experience and working in-house in
bio/pharmaceutical industry for a public company. This position
will oversee legal agreements and provide general dedicated legal
support to the Company's CMC and Quality functions, working on
clinical and commercial supply agreements and related strategic
considerations partnering with our CMC team. The candidate will
also support program & alliance management, and provide support for
our clinical operations team as needed. This is an exciting
opportunity for a dynamic and collaborative life sciences attorney
who wants to contribute to the growth of a thriving, fast-paced
biotech company. This position reports to the Chief Legal Officer
and will be in Boston, Massachusetts, USA. We will consider other
jurisdictions for exceptional candidates. The level of the position
will be commensurate with the candidate's education and industry
experience. This role is a hybrid position, requiring a minimum of
2 days per week in the office. RESPONSIBILITIES:
- Independently provide legal support, including support for
strategic contract agreements in support of the company's CMC and
Quality functions. It will also provide general legal support for
our program & alliance management function, as well as our clnical
operations function s needed, including confidentiality agreements,
material transfer agreements, consulting agreements, clinical and
commercial supply agreements as well as other general legal advice
and counsel.
- Independently negotiate and finalize agreements and support the
company's global contracting process to ensure the efficient and
effective delivery of contracting services to the business.
- Respond to internal inquiries concerning legal matter and
proactively identify and consider legal and other issues that may
arise from those questions. Where appropriate, consult with other
members of the Legal team and/or outside counsel before providing
advice.
- Partner and collaborate with Legal, Finance, and CMC groups, as
appropriate, to ensure cross-functional alignment through effective
communications and strong relationships.
- Identify, research and analyze legal risks and implications
with respect to the Company's existing and contemplated projects
and business transactions.
- Review existing templates, and establish new templates in
accordance with best practice and recent legal developments and
implement changes.
- Contribute to the development of policies and procedures to
ensure legal compliance; prepare and provide training on new
policies and/or procedures to key stakeholders and/or company-wide,
as appropriate.
- Liaise with external counsel on legal matters as required.
- Preparation of other legal documents as required.
- Act in accordance with Company policies, including, for
example, the Code of Business Conduct and Ethics and ensure
policies are understood and followed by direct reports, if
any.
- Some international travel may be required.
- Other duties as assigned. QUALIFICATIONS:
- JD (or its equivalent in selected jurisdictions) and minimum of
6+ years of legal experience; law firm experience preferred;
in-house with a bio/pharmaceutical company strongly preferred.
- Knowledge generally of relevant laws, regulations and guidance
specific to the bio/pharmaceutical industry.
- Ability to work flexibly with a strong work ethic and positive
attitude.
- Excellent interpersonal skills, including written and verbal
communication skills, with a customer-focused and professional
demeanor.
- Life-long learner of in-house legal department best practices
and standards. Able to leverage legal affairs peer groups to
determine best practices.
- Excellent analytical, problem-solving, and organizational
skills to handle multiple responsibilities. simultaneously and
still meet high quality and timeliness standards.
- Accountability, sound judgment, pragmatic business acumen and
the ability to take ownership of an issue and provide concise and
timely advice.
- Excellent interpersonal skills and a professional client
service orientation towards internal and external
stakeholders.
- Ability to work independently, as a team member, and across the
organization with varying levels of employees.
- Excellent research, writing, and communication skills
- Adept at technical tools, including Word, Excel, PowerPoint,
Microsoft Teams, and document sharing and e-signing toolsJD and
minimum of 6+ years of legal experience; law firm experience
required; in-house with a bio/pharmaceutical company strongly
preferred.
- Prior securities experience preferred as well as experience in
the life sciences, or similar, industry.
- Extensive knowledge of relevant laws, regulations, guidance,
and industry codes.
- Ability to work flexibly with a strong work ethic and positive
attitude.
- Excellent interpersonal skills, including written and verbal
communication skills, with a customer-focused and professional
demeanor.
- Life-long learner of in-house legal department best practices
and standards. Able to leverage legal affairs peer groups to
determine best practices.
- Excellent analytical, problem-solving, and organizational
skills to handle multiple responsibilities. simultaneously and
still meet high quality and timeliness standards.
- Accountability, sound judgment, pragmatic business acumen and
the ability to take ownership of an issue and provide concise and
timely advice.
- Excellent interpersonal skills and a professional client
service orientation towards internal and external
stakeholders.
- Ability to work independently, as a team member, and across the
organization with varying levels of employees.
- Excellent research, writing, and communication skills
- Advanced redlining skills with strong attention to detail.
- Adept at technical tools, including Word, Excel, PowerPoint,
Microsoft Teams, and document sharing and e-signing tools. The base
salary range for this role is$223,700 to $252,000 USD; we will
consider above this range for exceptional candidates. Base salary
is determined by a combination of factors including, but not
limited to, education and other qualifications, years of relevant
experience, and internal equity. Our Total Rewards program includes
base salary, target bonus, and stock options, as well as a full
range of benefits including medical, dental, vision, short-&
long-term disability, accidental death & dismemberment, and life
insurance programs, Employee Assistance Program, travel insurance,
and retirement savings programs with company matching
contributions.
Xenon encourages time to rest and re-charge through vacation,
personal days, sick days, and an end-of-year company shutdown.
Xenon highly values employee development and has an expanding
Training, Learning & Development program, including a Tuition
Assistance program for advanced degrees.
US positions only:Xenon Pharmaceuticals USA Inc. participates in
the E-Verify program in all states in which we hire. Learn more
about the E-Verify program here . To apply for this position, click
Apply Now to complete the application. We thank all applicants for
their interest; however, due to the volume of applicants, only
those chosen for interview will be contacted.
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Keywords: Dr. Phillips Center, Boston , Director, Legal, Executive , Boston, Massachusetts
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