Vir Biotechnology

Associate Director, Clinical Transactional Counsel

Vir Biotechnology$167K — $246K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • JD and 8+ years' experience in pharmaceutical or life sciences industry
  • Extensive experience in clinical contract negotiations
  • Proven track record in authoring and managing clinical trial agreements and MSAs
  • Ability to provide business-oriented guidance on clinical contracting issues
  • Knowledge of local regulations impacting clinical agreements
  • Experience supporting clinical trials throughout all stages
  • Understanding of outsourcing and procurement processes

Responsibilities

  • Lead negotiation and oversight of clinical study agreements and vendor contracts
  • Manage the clinical trial agreement process for global, multi-site trials
  • Collaborate with clinical operations and project leaders to align contracts with development priorities
  • Review and ensure compliance of clinical agreement templates with country regulations
  • Update negotiation playbooks based on recent contract escalations and market conditions
  • Work with Legal to assess and manage risks
  • Co-manage external partnerships with contract service providers and oversee governance reviews

Benefits

  • Comprehensive health and welfare benefit plans
  • Non-accrual paid time off and company shutdown for holidays
  • Commuter benefits
  • 401K match
  • Daily lunch provided in the office
Full Job Description
THE OPPORTUNITY

Vir Biotechnology is looking for an Associate Director, Clinical Transactional Counsel to manage the drafting, review and negotiation of clinical site agreements and vendor contracts. You will report to the Vice President, Strategic Transactions and work with the Clinical Operations team, Legal team and external partners to ensure clinical agreements comply with business best practices and relevant country regulations.

This role is located in our San Francisco headquarters with an expectation of 3 days per week in office.
WHAT YOU'LL DO
  • Direct negotiation, and oversight of negotiations, of clinical study agreements (including clinical trial agreements, confidentiality agreements and related contracts) and clinical vendors agreements (including master service agreements, MTAs and SOWs) in accordance with established development timelines
  • End-to-end management of the clinical trial agreement process and strategy for global, multi-site clinical trials
  • Partner closely with clinical operations, project leadership and additional functional leaders to understand development priorities to support delivery of negotiated contracts
  • Review established country specific templates for clinical trial agreements, confidentiality agreements, master service agreements, consulting agreements and other development agreements to ensure compliance with country regulations, align with business practices, market competitiveness and incorporate lessons learned
  • Review clinical trial agreement negotiation playbooks to assess recent escalations in site contracts, update terms following negotiations, ensure alignment with market conditions and to include new country specific regulations
  • Collaborate regularly with Legal for assessment of risk
  • Co-manage the external partnership with the site contract and budget functional service provider. Participation in bi-weekly status meetings, quarterly governance/KPI reviews and facilitate review and execution of annual service work orders


WHO YOU ARE AND WHAT YOU BRING
  • JD and 8+ years' experience in the pharmaceutical or life sciences industry; with extensive experience in clinical contract negotiations
  • Demonstrated experience in the authoring, negotiation and management of clinical trial agreements, master service agreements and other governing documents
  • Experience providing clear, practical, and business-oriented guidance on all clinical contracting issues throughout the contracting process
  • Knowledge of relevant local regulations
  • Experience providing contract support at several stages of clinical trials including start-up, maintenance and close-out
  • Knowledge of outsourcing and procurement processes to support contract execution, purchase orders and vendor invoice review


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WHO WE ARE AND WHAT WE OFFER

The expected salary range for this position is $167,500 to $246,500 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.

Vir Biotechnology's compensation and benefits are aligned with the current market and commensurate with the person's experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.

Applicants must currently be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

About Vir Biotechnology

Vir Biotechnology is a clinical-stage biotechnology company that develops treatments for infectious diseases. The company's platform uses monoclonal antibodies to target and neutralize viruses, including COVID-19, HIV, and hepatitis B. Vir's technology has the potential to improve patient outcomes and reduce healthcare costs by providing effective treatments for viral infections. The company was founded in 2016 and is headquartered in San Francisco, California.
Learn more about Vir Biotechnology
Size
444 employees
Market Cap
$3.3 billion
Industry
Net Income
-$298.6 million
Founded
2016
Revenue
$76.3 million
NASDAQ

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