Global Oncology Clinical Operations Lead

Virbiotechnologyinc; San Francisco (CA); On-site; USD 177,000 - 247,000; Full time

Job summary

Vir Biotechnology, Inc. in San Francisco seeks an Associate Director, Clinical Operations to independently lead global, complex oncology trials. You will manage the Study Management Team, oversee CROs and vendors, and ensure successful execution across early to late-stage development.

This role is based at our San Francisco headquarters with in-office expectations. You will lead study setup, timelines, budgets, and regulatory strategy, shaping core documents and cross-functional collaboration.

Qualifications

• Bachelor of Science degree is required, preferably in the life sciences.
• 10+ years of clinical development experience in the biotech/pharmaceutical industry.
• Extensive experience working on oncology clinical studies.
• Experience in managing and leading clinical studies from early phase to late stage.
• Experience in leading all stages of clinical trials including start up, maintenance and closeout.
• Thorough understanding of FDA, EMEA, and ROW ICH and GCP guidelines and cross-functional clinical processes.

Responsibilities

• Provide strategic input and leadership in study setup and execution of highly complex oncology clinical trials.
• Establish and monitor study timelines and budgets, escalates risks or changes as needed.
• Develop and manage study contracts, budgets and timelines.
• Author/review core study documents including protocol and informed consent forms.
• Manage CROs, central labs, systems vendors, and ancillary vendors to ensure on-target deliverables.
• Lead SOP development and cross-functional initiatives as needed.
• Support regulatory strategy and assess trial/program impact and RFIs from multiple countries.

Skills

Clinical Operations leadership

Vendor management

Global trials

Regulatory knowledge

Education

Bachelor of Science

Job description

Vir Biotechnology, Inc. in San Francisco seeks an Associate Director, Clinical Operations to independently lead global, complex oncology trials. You will manage the Study Management Team, oversee CROs and vendors, and ensure successful execution across early to late-stage development.

This role is based at our San Francisco headquarters with in-office expectations. You will lead study setup, timelines, budgets, and regulatory strategy, shaping core documents and cross-functional collaboration.