Director / VP, Clinical Evidence

MyOme; Menlo Park (CA); Hybrid; USD 170,000 - 250,000; Full time

Benefits offered by this job

Comprehensive healthcare coverage

401K

Unlimited PTO

Professional development opportunities

Company-sponsored off-sites

Job summary

A leading biotechnology firm in Menlo Park, CA is seeking a Clinical Development Lead to drive clinical strategy and oversee multi-site trials that will transform healthcare. Ideal candidates will possess an M.D. or PhD, along with over 5 years of clinical trial experience. Responsibilities include designing trials, navigating regulatory bodies, and analyzing clinical data. This hybrid role offers competitive compensation, comprehensive healthcare, and opportunities for career growth.

Qualifications

• At least 5 years of clinical experience preferred.
• Experience collaborating with academic institutions and research networks.
• Ability to operate in a fast-moving environment.

Responsibilities

• Develop and lead clinical strategy for company goals.
• Design and implement clinical trials.
• Navigate FDA for compliance with studies.
• Operationalize trials through contracting and budgeting.
• Analyze and interpret clinical data.

Skills

Clinical trial leadership

Regulatory requirements understanding

Clinical operations knowledge

Networking ability

Adaptability

Education

Medical degree (M.D. or D.O.) or PhD

Job description

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 as a clinical subject matter expert.

What You’ll Need

• Medical degree (M.D. or D.O.) with at least 5 years of clinical experience preferred or PhD with extensive trial experience.
• Proven experience in clinical trial leadership, including collaboration with academic institutions, research networks, and industry partners.
• Strong understanding of clinical operations, regulatory requirements (e.g. FDA), and trial design principles (pharma, device, diagnostics)
• Demonstrated ability to build wide and effective networks of contacts inside and outside the organization, across a diverse spectrum of people.
• Comfortable operating in a fast-moving environment, balancing strategic oversight with hands‑on execution.
• Open‑minded and adaptable, willing to roll up your sleeves and contribute wherever needed to move programs forward.

Location, Compensation, and Benefits

• Location: Ideally, this would be a hybrid position at our Menlo Park, CA office. Remote consideration based on experience and role fit.
• Compensation: Annual base salary range is $170,000 - $250,000, based on experience.

San Francisco Bay Area pay range: $170,000 USD - $250,000 USD

Benefits

• Comprehensive healthcare coverage (Health, Dental, and Vision)
• 401K
• Unlimited 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.

Learn More: myome.com