Oncology Clinical Scientist, Associate Director

Virbiotechnologyinc

San Francisco (CA)

On-site

USD 177,000 - 247,000

Full time

5 days ago
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Benefits offered by this job

Health benefits
Equity and bonus eligibility
401K match
PTO and holidays

Job summary

Vir Biotechnology, Inc. is seeking an Associate Director, Clinical Scientist, to drive execution of oncology studies in collaboration with Operations, Medical Monitoring, Data Management, Biostatistics, and Regulatory teams.

Based in San Francisco, this role emphasizes data-driven study design, execution, and reporting, with onsite presence three days per week. The ideal candidate will have a PhD/PharmD/MSN/NP/PA or equivalent and 7+ years in oncology clinical research, plus strong GCP/ICH

Qualifications

  • Advanced degree in Life Sciences, Nursing, Pharmacy, Medicine, or a related field.
  • 7+ years of experience in oncology clinical research.
  • Experience supporting 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 and collaborating with cross-functional study teams.
  • Knowledge of protocol development, clinical trial operations, and study execution.

Responsibilities

  • Serve as the Clinical Scientist for one or more oncology clinical studies, supporting 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.

Skills

Oncology clinical research
Cross-functional collaboration
GCP/ICH knowledge
Strong communication
Study design & analysis

Education

PhD, PharmD, MSN, NP, PA or equivalent

Job description

Vir Biotechnology, Inc. is seeking an Associate Director, Clinical Scientist, to drive execution of oncology studies in collaboration with Operations, Medical Monitoring, Data Management, Biostatistics, and Regulatory teams.

Based in San Francisco, this role emphasizes data-driven study design, execution, and reporting, with onsite presence three days per week. The ideal candidate will have a PhD/PharmD/MSN/NP/PA or equivalent and 7+ years in oncology clinical research, plus strong GCP/ICH

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