Vir Biotechnology

HQ
San Francisco
Total Offices: 3
611 Total Employees
Year Founded: 2016

Vir Biotechnology Benefits Overview

Compensation + Benefits

Offers 401(K)

Offers life insurance

Offers occupational accident insurance

Offers disability insurance

Offers supplemental life insurance

Offers accidental death & dismemberment insurance

Provides adoption assistance

Provides family medical leave

Offers childcare benefits

Offers generous parental leave

Offers company equity

Offers performance bonuses

Offers employee stock purchase plan

Offers employee discounts

Offers dental insurance

Offers health insurance

Offers mental health benefits

Offers dependent care

Offers Flexible Spending Account (FSA)

Offers vision insurance

Offers Health Savings Account (HSA)

Offers healthcare on-site

Company Culture

Provides commuter benefits

Provides a mobile phone discount

Provides free snacks and drinks

Offers travel concierge services

Offers a remote work program

Offers diversity-based Employee Resource Groups

Work-Life Balance + Wellbeing

Offers company-sponsored outings

Offers gym membership

Offers an Employee Assistance Program (EAP)

Offers generous PTO

Provides paid sick days

Provides military leave

Provides paid holidays

Provides bereavement leave

Offers unpaid extended leave

Career Growth + Development

Provides customized development tracks

Job training & conferences

Provides tuition assistance

Offers apprenticeship programs

5 Days AgoSaved
Remote or Hybrid
United States
Biotech
Perform regulatory writing and editorial/QC for submission documents (protocols, IBs, CSRs, briefing packages, NDA/IND/MAA components). Verify accuracy and consistency versus source data, apply style guides and templates, proofread and copyedit, prepare eCTD/CTD submission materials, communicate QC findings, manage document workflows and timelines, and improve QC tools and SOPs.
5 Days AgoSaved
Remote or Hybrid
United States
Biotech
Create, edit, and ensure compliance of regulatory submission documents (protocols, IBs, CSRs, Module 2/5 summaries) for global health authorities. Translate complex clinical data into clear text, coordinate cross-functional inputs, manage writing timelines, and advise teams on regulatory writing best practices to support IND/NDA/MAA and other submission activities.
5 Days AgoSaved
Remote or Hybrid
United States
Biotech
Lead and produce high-quality regulatory submission documents (protocols, IBs, CSRs, Module 2/5 summaries, labeling, briefing packages) for FDA/EMA. Ensure compliance with ICH/GxP, manage writing projects and timelines, collaborate with cross-functional teams, and define SOPs and best practices.