Sr. Director, Integrated Evidence Generation Lead (Oncology)

Location: Remote within any US state

Salary: $290,000–$300,000 per year, plus performance-based bonus and equity

Company

hirify.global is a biopharmaceutical company developing novel therapeutic candidates for unmet needs in oncology, with a focus on improving quality of life and survival for people with cancer.

What you will do

• Develop and maintain integrated evidence generation plans across the oncology portfolio and align them with product lifecycle objectives.
• Identify evidence gaps and coordinate strategy with Medical Affairs, Clinical Development, Commercial, Market Access, Health Economics, Regulatory, Legal, and Data Science.
• Design and oversee observational studies, retrospective cohorts, pragmatic trials, external control arms, registries, and database analyses using claims, EHR, oncology, molecular, and patient-reported data.
• Lead protocol and analysis plan development, providing scientific and epidemiologic oversight and ensuring rigorous use of real-world endpoints.
• Oversee Expanded Access Programs and Investigator-Sponsored Research, including governance, compliance, budgets, contracts, and investigator engagement.
• Manage end-to-end project delivery, vendors, CROs, budgets, timelines, quality, data privacy, regulatory interactions, and external scientific partnerships.

Requirements

• Advanced degree such as PhD, MD, PharmD, DrPH, or ScD in epidemiology, biostatistics, oncology, public health, or a related field; a master's degree with additional experience may be acceptable.
• At least 12 years of relevant experience for the Senior Director level, including demonstrated leadership of enterprise-level real-world evidence programs and at least 5 years in oncology.
• Proven experience designing and delivering observational studies and real-world evidence supporting regulatory interactions, label decisions, market access, reimbursement, or clinical development.
• Deep knowledge of oncology clinical endpoints and treatment paradigms; NSCLC experience is preferred.
• Hands-on experience with EHR, claims, molecular/genomic registries, clinical registries, data linkage, advanced epidemiologic methods, and causal inference.
• Experience managing vendors, CROs, multidisciplinary teams, projects, budgets, regulatory stakeholders, payers, KOLs, and external collaborators; willingness to travel as needed.

Nice to have

• NSCLC background.
• Publication and conference presentation record.
• Master's degree with substantial relevant experience where an advanced degree is not held.

Culture & Benefits

• Competitive base salary, annual performance-based bonus, and equity or long-term incentive units.
• Unlimited vacation and 10 sick days annually.
• Medical, dental, and vision coverage.
• 401(k) with company matching.
• Action-oriented, collaborative environment with an emphasis on accountability, adaptability, communication, and scientific credibility.