# Senior Clinical Trial Manager at MyOme > Remote · region unclear · Manager · Software engineering · open. Source: https://alderhq.app/jobs/greenhouse%3Amyome%3A4363116009 (read 2026-11-13). ## Facts (observed) - Company: [MyOme](https://alderhq.app/companies/myome) - Location text: Remote; Remote - Where it can be done from (inferred): Remote · region unclear (evidence: "Location: Remote; Remote") - Posted: 2026-08-11 (94 days ago) - First seen by alder: 2026-11-07 · last verified: 2026-11-07 - Reposted: 0 times · edited: 0 times - Apply on the employer's site: https://myome.com/about-us/careers?gh_jid=4363116009 ## Pay and sponsorship - Posted pay: $145k–$185k per year (from the listing's pay field) ## Description (the employer's text) MyOme is a clinical whole genome analysis company helping individuals and families understand their risk for disease. As a leader in polygenic and AI-based integrative risk modeling, we combine genome sequencing with AI-driven analytics and clinical data to deliver a lifetime of clinically meaningful, actionable insights, from proactive risk assessment to rare disease diagnosis. Our laboratory is CLIA-certified and CAP-accredited, and we’re based in Menlo Park, California. Our team brings together scientists, engineers, clinicians, and professionals across disciplines, united by a shared purpose: making genomic insight a routine part of everyday healthcare. We put patients first and hold ourselves to the scientific and clinical rigor that families and their clinicians depend on. Joining MyOme means contributing your expertise to work that matters for patients and families. Whether you’re advancing our science and technology, supporting the clinicians and patients we serve, or strengthening our operations, you’ll help turn genomic discoveries into better care. ### Position Overview The Senior Clinical Trial Manager is a key contributor to MyOme’s clinical evidence generation strategy with responsibility for executing assigned clinical studies within agreed upon timelines and budgets. This is a highly cross-functional role that partners closely with internal stakeholders and external partners to translate evidence needs into actionable clinical protocols and oversees their execution by CROs, supporting vendors, and study sites. You must have substantial experience successfully managing clinical studies through CROs. ### What You'll Do - Own study execution within agreed upon timelines and budget, ensuring compliance with Good Clinical Practice, applicable regulatory requirements, study protocols and MyOme SOPs. - Leads the execution of studies from feasibility to delivery of analysis-ready datasets. - Leads the identification and selection process for CROs and other vendors supporting study execution. - Primary point of contact for vendors involved in study execution. - Oversees study budgets, reviewing and approving vendor invoices, tracking spend versus plan in partnership with Accounting and Finance - Contributes to the development of study-related documents including protocols, informed consent forms, laboratory manuals, monitoring plans, communication plans, training materials and SOPs - Leads the internal, cross-functional study team and acts as the driver for escalation of issues to MyOme management that may impact study delivery on-time and on-budget. - Leads the cross-functional study risk review process, proactively identifying and managing operational risks. - Collaborates with key stakeholders across MyOme and provides periodic updates on study progress ### What You'll Need - Bachelor’s degree in a life science, health-discipline or related field. Advanced degree (e.g., MS, MPH, MSN, PharmD, PhD) preferred. - A minimum of 8 years of clinical trial management experience, with at least 5 years running IVD clinical studies - Experience with interventional diagnostic studies and/or cancer early detection studies preferred. - Experience managing large (5,000+ participant) studies preferred. - Demonstrated success managing CROs and other clinical study vendors as the primary point of accountability on large, multi-site studies. - Strong working knowledge of FDA regulation and Good Clinical Practice guidelines for diagnostic studies. - Strong analytical, problem-solving, communication, and stakeholder management skills. - Proven ability to manage study budgets, timelines and cross-functional teams with minimal oversight, PMP certification preferred. - Excellent communication, negotiation and stakeholder management skills. - Willingness to travel up to 20% ### Location, Compensation, and Benefits - Location: Remote in the US - Compensation: Annual salary range is $145,000 - $185,000, based on experience. This role is also eligible for equity. San Francisco Bay Area pay range $145,000—$185,000 USD ### Benefits - Comprehensive healthcare coverage (Health, Dental, and Vision) --- Data: alder (https://alderhq.app). Cite https://alderhq.app/jobs/greenhouse%3Amyome%3A4363116009 and the date you read it. Observed facts come from the employer's own listing; location reach, level, family and skills are inferences.