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 Bio is looking for a temporary Project Manager to support cross-functional workstream and project management activities for a clinical-stage asset being transitioned to a strategic partner. The ideal candidate brings strong foundational project management skills, experience in clinical development and regulatory processes, and comfort working on partnered assets in a dynamic, fast-paced environment. The Project Manager will support the transition of program-related contracts and related purchase orders, ensuring vendors are notified following the terms of the respective agreements and appropriately tracked for a clean transfer of responsibilities between Vir Bio and partner budgets, invoices, and financial reporting. The role will work closely with Alliance Management, Finance, Legal, Procurement, Development Operations, Clinical Operations and CMC/Manufacturing to ensure a clean cutoff of regulatory and legal ownership, and disciplined trancing of contracts for timely transfer.

This role is based at our San Francisco headquarters, with an expectation of at least three days per week in the office. 

WHAT YOU'LL DO

Maintain an integrated tracker of all transition-related contracts, POs and any other financial obligations
Support mapping of each contract to the appropriate functional owner, transition status, etc.
Support financial lead in separating pre-cutoff and post-cutoff financial obligations
Coordinate with function owners to confirm termination or transfer readiness
Coordinate with legal to confirm contractual obligations related to transfer
Follow-up with functional stakeholders across AM, Legal, Procurement, Clinical Operations, Clinical Research, Development Operations and CMC on missing information or unresolved transition terms
Prepare weekly status updates, dashboards, and issues log
Support meeting preparation, agenda setting, action item tracking
Support post-transfer reconciliation and track remaining obligations and disputed or unclear expenses

WHO YOU ARE AND WHAT YOU BRING

BS/BA in a scientific or related discipline required; advanced degree (MS, PharmD, PhD, MBA) a plus
12+ years of experience in the biopharmaceutical industry, with 5+ years in project management or equivalent cross-functional coordination roles
Experience supporting clinical development programs and familiarity with key regulatory milestones and submissions
Familiarity with contracts, budgets, invoices and POs. Strong attention to detail and ability to manage multiple workstreams under a tight timeline
Experience working on partnered or co-development programs strongly preferred; financial integration experience is a plus
Solid project management fundamentals: planning, scheduling, risk/issue management, stakeholder communication, and meeting facilitation
Experience with digital tools for project planning, tracking and collaboration, including Smartsheet, SharePoint, Microsoft Office products, and other widely used project management platforms
Demonstrated ability to work effectively with cross-functional teams
Comfortable operating in a fast-paced, evolving environment, balancing tactical execution (agendas, minutes, trackers) with broader project planning and coordination

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WHO WE ARE AND WHAT WE OFFER

The expected hourly range for this position is $ 58,00 to $109.00 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.

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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Associate Director, Project Management (Temporary)