Associate Director, Clinical Scientist

Vir Biotechnology • San Francisco, CA

6d • Hybrid

About The Position

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 an Associate Director, Clinical Scientist, to play a key role in the execution of oncology clinical studies, partnering closely with Clinical Operations, Medical Monitoring, Data Management, Biostatistics, and Regulatory teams to support study startup, conduct, analysis, and reporting. This is a highly collaborative and hands-on role for an experienced clinical scientist who enjoys being close to the data, contributing to study design and execution, and helping advance programs from early development through key clinical milestones. This role is based in our San Francisco headquarters with an expectation of being onsite at least three days per week.

Requirements

• Advanced degree in Life Sciences, Nursing, Pharmacy, Medicine, or a related field (PhD, PharmD, MSN, NP, PA, or equivalent) preferred
• 7+ years of experience in oncology clinical research within biotechnology, pharmaceutical, CRO, or academic environments
• Experience supporting the design, conduct, and analysis of oncology clinical trials
• Strong understanding of GCP, ICH guidelines, and the clinical drug development process.
• Experience reviewing clinical trial data, identifying trends, and collaborating with cross-functional study teams
• Knowledge of protocol development, clinical trial operations, and study execution
• Strong communication, organizational, and problem-solving skills with the ability to manage multiple priorities in a fast-paced environment
• Collaborative, detail-oriented, and committed to delivering high-quality work

Responsibilities

• Serve as the Clinical Scientist for one or more oncology clinical studies, supporting study startup, execution, data review, and reporting activities
• Partner cross-functionally with Clinical Operations, Medical Monitoring, Data Management, Biostatistics, Regulatory, and other teams to support successful study conduct
• Contribute to protocol and informed consent development, including authoring, review, and resolution of cross-functional feedback
• Perform ongoing clinical data review, identify trends and potential issues, and collaborate with study teams to ensure high-quality data
• Support site-facing activities, including investigator meetings, study training, and responses to protocol-related questions
• Contribute to the preparation and review of clinical study reports, regulatory submissions, safety reports, and other clinical documents
• Participate in the review and interpretation of emerging clinical data and support study analyses and presentations

Benefits

• compensation
• bonus
• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level