Senior Scientist, Clinical Biostatistics & Genetic Risk Prediction
Position Overview
The position involves designing and analyzing clinical studies to establish the utility of MyOme's risk prediction models in real clinical settings. The role requires ownership of trial design, estimands, and Statistical Analysis Plans, and direct involvement in data analysis.
What You'll Do
- Design prospective, biomarker-stratified studies to demonstrate the clinical utility of our models
- Define estimands, endpoints, and analysis strategies
- Develop and execute Statistical Analysis Plans, sample-size and power calculations, and primary, sensitivity, and subgroup analyses consistent with ICH E9 / E9(R1)
- Pull, clean, and analyze complex data (e.g., biobank cohorts, EHR extracts, registries) in reproducible and well-structured code
- Apply statistical genetics methodology (calibration, ancestry portability, confounding, population stratification) to study design and score evaluation
- Partner with medical, regulatory, and clinical operations teams and support trial-related regulatory interactions
What You'll Need
- Ph.D. in Biostatistics, Statistical Genetics, Genetic Epidemiology, or a related quantitative field and 4+ years of professional experience in a similar role
- Demonstrated clinical study / trial design experience: SAP authorship, sample-size/power, estimands, and working command of ICH E9
- Statistical genetics or genetic epidemiology experience
- Demonstrated ability to take raw, poorly-structured data and produce clean, reproducible analyses independently
- Proficiency in Python and/or R, version control (Git), and large genomic/clinical datasets in cloud environments (AWS / GCP / DNAnexus)
- Survival and longitudinal modeling; causal inference for observational data
- Strong written and verbal communication skills to communicate complex statistical concepts to non-technical audiences
Preferred / Bonus Qualifications
- Experience in a start-up environment
- Population-scale biobank experience (UK Biobank, All of Us, MVP)
- Strong publication record that demonstrates initiative and scientific independence
- Direct work on a genetics clinical-utility or decision-impact study
- Regulatory trial experience (IDE, FDA interactions) or clinical validation for diagnostics / SaMD
Location, Compensation, and Benefits
Location: Hybrid, 2–3 days onsite at our Menlo Park, CA office; Bay Area candidates preferred. Remote in the US considered for the right candidate.
Compensation: Annual salary range of $160,000 - $180,000, commensurate with experience. This role is also eligible for equity.
San Francisco Bay Area pay range: $160,000 USD - $180,000 USD
Benefits: Comprehensive healthcare coverage (Health, Dental, and Vision), 401K, Unlimted PTO, Professional development opportunities, Company-sponsored off-sites and team meals during in-person meetings, Direct access to company leadership and the opportunity for career growth
Diversity, Inclusion, and Equal Opportunity
MyOme values diversity in all forms. We believe that diverse perspectives drive better science and better patient outcomes. We are an Equal Opportunity Employer committed to creating an inclusive workplace that empowers every individual.
Why Work at MyOme?
Join us if you: Want to make an impact at the intersection of healthcare and technology, changing the way people engage with their health at the genetic level Enjoy rolling up your sleeves, taking initiative, and being empowered to lead Value humility, transparency, and collaborative problem-solving Thrive in fast-moving, dynamic environments with smart, driven teammates Appreciate competitive compensation, meaningful equity, and excellent benefits
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