Director, Clinical Transactional Counsel

Vir Biotechnology, Inc.; San Francisco (CA); On-site; USD 120,000 - 284,000; Full time

Benefits offered by this job

Bonus and equity

Health benefits

Paid time off

Company holidays

Commuter benefits

401K match

Lunch provided

Job summary

Vir Biotechnology, Inc. is seeking a Director, Clinical Transactional Counsel to lead drafting, reviewing, negotiating, and executing clinical agreements for global development programs.

This hands-on role partners with Clinical Operations, Procurement, Finance, and Legal to drive efficient study startup and execution while managing risk. The position is based at our San Francisco headquarters with an expectation of three days per week in the office.

Qualifications

• JD and 10+ years in pharma/biotech or life sciences, with significant clinical contracting experience.
• Independent drafting, reviewing, and negotiation of high-volume clinical trial and vendor agreements.
• Experience supporting global development programs across multiple countries and regions.
• Strong understanding of clinical research regulations and contracting requirements by country.
• Ability to balance legal risk with business needs and provide practical guidance.
• Experience collaborating with Clinical Operations, Development, Legal, Procurement, and Finance stakeholders.

Responsibilities

• Negotiate clinical study agreements, confidentiality agreements, amendments, and related documents.
• Draft, review, negotiate, and manage vendor contracts including master service agreements and statements of work.
• Own end-to-end contracting process for global multi-site trials to support milestones.
• Serve as primary contracting partner to cross-functional teams.
• Provide risk-based guidance and resolve negotiation escalations.
• Improve templates, playbooks, and standard language with evolving regulations.
• Identify contracting risks with stakeholders and ensure terms support operations.
• Oversee external site contracting and budget vendor governance and KPI reviews.
• Monitor regulatory changes and update contracting processes accordingly.
• Drive efficiency, consistency, and scalability across Vir's global portfolio.

Skills

Negotiation of CTAs

Communication

Project management

Stakeholder management

Education

Juris Doctor (JD)

Job description

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 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

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.

• compensation, bonus and equity
• health and welfare benefit plans
• non‑accrual paid time off
• company shut down for holidays
• commuter benefits
• 401K match
• 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.