Associate Director / Director of Product Management (Hematologic Oncology)

Location: US Remote; must be based in the United States. Pacific time hours are required; site-based presence in San Carlos, CA, Boulder, CO, or Austin, TX is preferred. Travel: 30–40% for advisory boards, congresses, and customer meetings.

Salary: $180,300–$230,900 USD annually.

Company

hirify.global develops cell-free DNA testing and personalized genetic diagnostics for oncology, reproductive health, and organ transplantation.

What you will do

• Own and execute the Sighirify.global product roadmap for hematologic malignancies, starting with multiple myeloma and lymphomas.
• Lead LDT market-entry planning, including clinical validation, CLIA and state requirements, reimbursement, payer considerations, and launch readiness.
• Define assay, sample, workflow, and reporting requirements with R&D, Lab Operations, and Software Engineering.
• Support IUO and IVD clinical trials, trial start-up, study requirements, and pharma or companion diagnostic opportunities.
• Build product metrics and dashboards covering volume, adoption, ordering patterns, turnaround time, and retention.
• Lead evidence-generation, market research, KOL engagement, product positioning, business cases, and executive recommendations.

Requirements

• Bachelor’s degree in life sciences, statistics, engineering, or a related field; MS, PhD, or MBA preferred.
• At least 5 years of experience, with 7+ preferred, in product management, product marketing, or market analytics within diagnostics, biotech, or pharmaceutical companies.
• Experience in hematologic oncology, especially multiple myeloma and lymphoma, is strongly preferred.
• Working knowledge of oncology molecular testing, NGS, biomarkers, bioinformatic workflows, variant calling, filtering, interpretation, and genomic data analysis.
• Experience with clinical trials and IUO and IVD regulated environments is required.
• Experience bringing a molecular test to market as an LDT, including clinical validation and laboratory requirements.
• Experience designing or supporting clinical validation studies, retrospective studies, or prospective trials.
• Understanding of MRD, whole genome sequencing, somatic and structural variants, single nucleotide variants, and phased variants in hematologic malignancies.
• Strong analytical, communication, organization, time-management, financial-modeling, and cross-functional leadership skills; proficiency with Excel, Word, and PowerPoint.

Nice to have

• Experience with data analysis tools such as SQL or Snowflake.
• Familiarity with high-complexity molecular laboratories, cfDNA, or plasma workflows.
• MRD experience, prior KOL engagement, and external customer-facing experience.
• Advanced degree in a relevant field.

Culture & Benefits

• Remote home-office work with occasional work outside normal hours and required availability during Pacific time hours.
• Highly matrixed collaboration across product, R&D, laboratory, software, medical, commercial, regulatory, and business development functions.
• Medical, dental, vision, life, disability, fertility, pregnancy and baby-bonding, 401(k), and commuter benefits for eligible employees and dependents.
• Employees and immediate families receive free testing, and the company provides an employee referral program.