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Director / VP, Clinical Evidence

MyOme - Menlo Park, California, United States

Posted Nov 20, 2025

Benefits

Parental leave
Not verified
Non-birth-parent leave
Not verified
Family-building benefits
  • Fertility benefits: Not verified
  • Adoption assistance: Not verified
  • Surrogacy assistance: Not verified
Mental health support
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Relocation assistance
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Childcare support
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Learning budget
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Verification
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Salary
$170K-$250K Verified - from the job posting source checked Jun 20, 2026
401(k) match
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Market context

U.S. role benchmark (BLS OEWS)
$81,444 U.S. median for this role
Projected growth (BLS Employment Projections)
+6.9% - Faster than average

158% above the BLS role benchmark for healthcare aggregate.

Matched to SOC 29-1141 - Healthcare aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Schedule

Shift type
Not verified
Weekend work
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Company

Company stage
Early Verified - from the job posting source checked Jun 20, 2026
Equity
Offered Verified - from the job posting source checked Jun 20, 2026

Application

Cover letter
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Assessment
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Deadline
Not stated

Where they hire

State eligibility is not yet verified.

About this role

Director / VP, Clinical Evidence Menlo Park, California, United States MyOme's mission is to provide clinically actionable genetic information to patients throughout their lives. We combine clinical-grade whole genome sequencing, advanced AI methods for genome interpretation, and seamless digital tools for doctors and patients to order and access results. Our team is composed of seasoned entrepreneurs, scientists, and operators, and we're backed by top-tier investors. Position Overview: This position drives direction and leadership for clinical development of several large-scale multi-site prospective trials (including one that is 50K+), which will transform healthcare. You will be accountable for the execution and aspects of design of our clinical evidence strategy, including protocol design, operationalizing the effort, and leading FDA interactions that relate to clinical utility. What You'll Do: - Develop and lead clinical strategy to advance company goals and evidence generation, including regulatory and reimbursement efforts. - Design and implement clinical trials, incorporating input from key opinion leaders and the clinical advisory board to optimize study interventions and endpoints. - Navigate FDA and other regulatory bodies to ensure compliance and successful study execution. - Operationalize trials through contracting, budgeting with large health organizations, and CROs. - Partner with internal teams (e.g., R&D) and consultants to ensure studies are appropriately powered and aligned with overall development strategy. - Provide clinical oversight and medical monitoring for ongoing studies. - Analyze and interpret clinical data, integrating findings into product development plans and regulatory submissions. - Represent the organization in external meetings with investigators, regulators, and collaborators

Read the full description at myome.com. FewerJobs shows a preview and links to the original posting.

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