Senior Manager, HTA, Value and Evidence (HV&E), Genitourinary Cancer

Location: New York City, United States; hybrid work onsite 2–3 days per week. The position may be based at any hirify.global site in North America or Europe, requires the ability to work across all US time zones, and involves domestic and international travel. Permanent U.S. work authorization is required.

Annual base salary: $139,100–$231,900, plus a 17.5% bonus target and eligibility for a share-based long-term incentive program.

Company

hirify.global is a biopharmaceutical company developing and delivering medicines and vaccines to improve patient health and access to treatment.

What you will do

• Support global HTA, Value & Evidence strategy development for the genitourinary cancer portfolio.
• Manage clinically relevant and scientifically valid Value & Evidence studies, including non-interventional studies and registries.
• Lead updates to global value dossiers, economic models, and other tools supporting product value propositions.
• Develop and execute real-world evidence strategies to support brand differentiation and patient access.
• Coordinate evidence needs from country and regional Access & Value teams with global strategy and project execution.
• Lead data dissemination plans, publications, and conference presentations for healthcare stakeholders.

Requirements

• Graduate degree required in health economics, health services research, epidemiology, pharmacy administration, pharmaceutical policy, or a related research-focused public health field.
• At least 2 years of relevant experience with an MSc, MPH, or MBA, or at least 1 year with a PharmD, PhD, or DrPH.
• Advanced knowledge of HEOR, health economics, patient-reported outcomes, study design, database analysis, epidemiology, statistics, and healthcare market trends.
• Strong project management skills, including contracting, budgeting, and vendor management.
• Ability to oversee small project teams, guide external stakeholders, manage complex projects, and influence within a matrix organization.
• Excellent written and spoken English communication skills required.

Nice to have

• Experience with clinical trials, patient-reported outcomes, and real-world study design and implementation.
• Oncology experience and familiarity with the biotech or pharmaceutical industry.
• Experience with HTA organizations such as NICE, CADTH, PBAC, ICER, and EU JCA.
• Completion of an HEOR-related fellowship.

Culture & Benefits

• Hybrid work with onsite attendance 2–3 days per week.
• Collaboration across global Oncology, Access, Medical, Clinical, Commercial, and country teams.
• 401(k) matching and an additional retirement savings contribution.
• Paid vacation, holidays, personal days, caregiver/parental leave, and medical leave.
• Medical, prescription drug, dental, and vision coverage.

Hiring process

• Local pay information for secondary posting locations is provided during the first interview where applicable.
• Employment eligibility and work authorization are verified as part of the hiring process.