Associate Director, Biosample Operations

Posted 13 Hours Ago
Be an Early Applicant
San Francisco, CA
Hybrid
169K-246K Annually
Senior level
Biotech
The Role
The Associate Director of Biosample Operations will manage project activities related to biomarker strategies within clinical programs, ensuring continuity and integrity across projects. Responsibilities include overseeing biosample collection, coordinating assay development, and managing vendor operations. This role supports clinical operations with a focus on ensuring compliance and efficient biomarker sample management.
Summary Generated by Built In

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. Vir’s clinical-stage portfolio includes infectious disease programs for chronic hepatitis delta and chronic hepatitis B infections, in addition to multiple oncology programs. Vir also has a preclinical portfolio of programs across a range of other infectious diseases and oncologic malignancies. 

We believe the success of our colleagues drives the success of our mission. We are committed to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give their best, we will collectively deliver outstanding results.

 

THE OPPORTUNITY:

Supporting the development portfolio, the Associate Director, Biosample Operations will planall project management and operational activities required to operationalize the VIR biomarker strategies (PK, ADA, PD, Exploratory Biomarker and CDx) for programs across the VIR portfolio. You will ensure continuity and integrity across projects, coordinate assay development and implementation activities and acts as the primarycontact for projects requiring biomarker and diagnostic activities including collection, delivery and assay testing of all biosamples within one or more clinical projects or clinical studies. You will  also be responsible for any biomarker and CDx sub-team meeting management, dashboards, following up on actions, organizing meetings and tracking biomarker deliverables.  In addition to the core biomarker activities, you will be involved in some clinical operation activities for clinical site management in the context of biomarker sample collection education and compliance at clinical sites.

This role will report to the VP, Clinical Operations Oncology

This role is located in our San Francisco headquarters with an expectation of 4 days per week in office.

WHAT YOU'LL DO:

  • Drive the implementation and execution of the clinical biomarker and diagnostic plans for therapeutic programs in early and late stage clinical development across therapeutic areas
  • Accountable for project management and appropriate planning of related biomarker analysis and samples management costs within a project(s) or clinical studies
  • Plan and implement the PK and biomarker and diagnostics biosamples collection within a project(s) or clinical study including definition of the appropriate material, instructions, lab manual development Kit development, database set up, etc
  • Ensure the timely and efficient delivery of all biosample, including scheduling analyses with relevant vendors, sample processing and shipment, analysis, data delivery and final sample disposition.
  • Serve as vendor operations lead with central lab and other ancillary labs and will oversee sample shipment and coordination of sample analyses, data transfers and sample reconciliation
  • Be the first contact for PK biomarker and diagnostics biosamples operational questions and issues within a project(s) and coordinates with internal and external partners
  • Provide guidance during protocol, informed consent form and CRF development to ensure feasibility of biological sampling and alignment with ICH/GCP, sample testing plans and data collection and reconciliation
  • Develop and implement a global strategy for standardization of clinical sample management for inspection readiness including development of SOPs for practices across clinical programs
  • Accountable for training, managing, and providing oversight of Biomarker Operations team and driving the overall biomarker operational strategy for the pipeline


WHO YOU ARE AND WHAT YOU BRING:

  • Life Science Degree or Higher At least 7+ years related professional experience in a clinical research setting, clinical/diagnostic laboratory, or pharmaceutical/biotechnology R&D environment
  • 3+ years Clinical or biological laboratory experience with involvement in the processing or analysis of biological samples 
  • Clinical development experience working on a crossfunctional team responsible for the execution of clinical studies, oncology preferred
  • Competent in application of standard business procedures (standard operating procedures, International Conference on Harmonization {ICH}, Global Regulations, Ethics and Compliance)
  • Project management skills and knowledge of project management tools


WHO WE ARE AND WHAT WE OFFER:

The expected salary range for this position is $168,500 to $246,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.

Vir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and 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.

Vir Biotechnology (“Vir”) is an equal opportunity employer.  All employment decisions at Vir are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to race, color, religion, sex (including pregnancy), gender, gender identity, gender expression, sexual orientation, age, parental status, marital status, national origin, ancestry, disability, medical condition, genetic information (including family medical history), political affiliation, military service or any other legally protected characteristic. 

This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs.  Vir also strongly commits to providing employees with a work environment free of unlawful discrimination or harassment.

Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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, Inc., participates in E-Verify.

Candidate Privacy Notice

 

The Company
611 Employees
Hybrid Workplace
Year Founded: 2016

What We Do

Vir Biotechnology, Inc. (in Europe, Humabs BioMed, https://bit.ly/46lQGN2) is an immunology company focused on powering the immune system to address unmet patient needs in infectious disease and beyond. Our powerful R&D engine combines our proprietary monoclonal antibody (mAb) platform with machine learning and artificial intelligence-enhanced capabilities, enabling us to engineer our rich database of human antibodies and deliver transformative medicines for diseases with significant global burden.

Our current pipeline consists of multiple clinical candidates targeting hepatitis B and hepatitis delta viruses and human immunodeficiency virus, including a potential functional cure for chronic hepatitis B and treatment for chronic hepatitis delta. Our portfolio of broad, potent investigational monoclonal antibodies also targets influenza A and B viruses, COVID-19, respiratory syncytial virus/human metapneumovirus and human papillomavirus, and our investigational T cell vaccine aims to prevent HIV. Explore our full pipeline: https://bit.ly/3tr7FPm

We collaborate with some of the world’s leaders in industry as well as government agencies and non-profit organizations enabling us to rapidly advance cutting-edge scientific discoveries and innovative technologies with the potential to benefit people around the world.

We are proud to have been ranked the fastest-growing company in North America on the 2022 Deloitte Technology Fast 500™.

Join us as we pursue our mission to transform lives.

It has come to our attention that there have been various recruitment scams targeting job seekers on LinkedIn. Vir Biotechnology, Inc. is committed to your privacy and will never request sensitive personal information including banking details through email, text message, social media or video software platforms. We also will never request a financial commitment from a candidate as part of the application process. Learn more about Vir’s recruiting process: https://bit.ly/461EgJN

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