Aimed at senior legal professionals with clinical contracting expertise who can manage global, multi-site trials and collaborate across departments.
Derived from job-description analysis by Serendipath's career intelligence engine.
Original posting from Vir Biotechnology via Greenhouse
Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN® dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.
Vir Biotechnology has exclusive rights to the universal PRO-XTEN® masking platform for oncology and infectious disease. PRO-XTEN® is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.
We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.
THE OPPORTUNITY
Vir Biotechnology is seeking a Director, Clinical Contracts-Transactional Counsel to lead the execution of clinical contracting activities supporting our global development programs. Reporting to the Vice President, Strategic Transactions, this role will serve as the primary legal and business partner for clinical contracting matters across clinical trial sites and external vendors.
This is a hands-on position responsible for personally managing the drafting, review, negotiation, and execution of a broad range of clinical agreements. The successful candidate will combine deep clinical contracting expertise with practical business judgment to support efficient study startup and execution while appropriately managing risk.
This role is based in our San Francisco headquarters with an expectation of 3 days per week in the office.
WHAT YOU'LL DO
Lead and conduct negotiations of clinical study agreements, including clinical trial agreements, confidentiality agreements, amendments, informed consent-related documents, and other site-facing agreements
Draft, review, negotiate, and manage vendor contracts, including master service agreements, statements of work, material transfer agreements, consulting agreements, and other development-related agreements
Own the end-to-end clinical contracting process for global, multi-site clinical trials, ensuring timely execution in support of development milestones
Serve as the primary contracting partner to Clinical Operations, Clinical Development, Procurement, Finance, and Legal teams
Provide practical, risk-based guidance on contractual issues and drive resolution of negotiation escalations
Own and continuously enhance clinical contracting templates, negotiation playbooks, and standard agreement language, incorporating lessons learned from negotiations, evolving regulatory requirements, and industry best practices
Partner closely with internal stakeholders to identify contracting risks, develop solutions, and ensure agreement terms support operational execution
Oversee day-to-day management of external site contracting and budget vendors, including governance meetings, KPI reviews, and service work order execution
Monitor changes in applicable regulations and industry practices and incorporate updates into contracting processes and templates
Drive continuous improvement of clinical contracting processes, templates, and negotiation playbooks to enhance efficiency, consistency, and scalability across Vir's global clinical portfolio
WHO YOU ARE AND WHAT YOU BRING
JD and 10+ years of experience in the pharmaceutical, biotechnology, or life sciences industry, with significant experience negotiating clinical trial agreements and related development contracts
Deep expertise independently drafting, reviewing, negotiating, and managing a high volume of clinical trial and vendor agreements
Demonstrated experience supporting global clinical development programs across multiple countries and regions
Strong understanding of clinical research regulations and country-specific contracting requirements
Ability to balance legal risk with business and operational priorities while providing practical, solution-oriented guidance
Experience collaborating with Clinical Operations, Development, Legal, Procurement, and Finance stakeholders in a fast-paced environment
Knowledge of outsourcing models, vendor governance, procurement processes, and contract execution workflows
Excellent negotiation, communication, project management, and stakeholder management skills
Proven ability to independently manage a complex and diverse portfolio of contracting activities with minimal supervision
#LI-AS1
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WHO WE ARE AND WHAT WE OFFER
The expected salary range for this position is $1203,500 to $284,000 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.
All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.
This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs. Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.
Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.
For hires based in the United States, Vir Biotechnology, participates in E-Verify.
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