Associate Director, Health Economics & Outcomes Research at Secura Bio

, , United States -

Full Time

Start Date

Immediate

Expiry Date

12 Jun, 26

Salary

235000.0

Posted On

14 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Health Economics, Outcomes Research, Real-World Evidence, Medical Affairs, Data Generation, Evidence Strategy, Hematologic Oncology, Observational Studies, Registries, Health Economic Analyses, Scientific Communication, Cross Functional Collaboration, Vendor Management, Project Management, Scientific Rigor, Compliance

Industry

Pharmaceutical Manufacturing

Description

About the Role Secura Bio is seeking a talented and motivated Associate Director of Health Economics and Outcomes Research to join our Medical Affairs organization. The ideal candidate will contribute to the generation, interpretation, and communication of outcomes and real-world evidence to support medical strategy, scientific exchange, and the articulation of clinical and patient value across the product lifecycle. As a key member of Medical Affairs, the Associate Director, HEOR will work closely with Medical Directors, Medical Science Liaisons (MSLs), Clinical Development, Biostatistics, and Market Access to ensure that robust, clinically relevant, and methodologically sound HEOR evidence supports disease education, external scientific dialogue, and evidence based decision making. Employment Type Full-time Reports To Senior Director, Global Medical Affairs Lead Key Responsibilities HEOR & Evidence Strategy (Medical Affairs–Led) Lead the development and execution of Medical Affairs aligned HEOR and real-world evidence (RWE) data generation for hematologic oncology assets across prelaunch and postlaunch phases. Lead and identify evidence gaps relevant to clinical practice, treatment pathways, and patient outcomes in hematologic malignancies (e.g., lymphoma, leukemia, multiple myeloma). Provide strategic input into Medical Affairs plans, including integrated evidence generation and scientific communication strategies. Outcomes Research & Real-World Evidence Design and oversee observational studies, registries, chart reviews, and other RWE initiatives relevant to hematologic oncology populations. Partner with Clinical and Biostatistics teams to ensure alignment between clinical trial data and RWE generation. Health Economics & Value Context Oversee the development and interpretation of health economic analyses (e.g., cost effectiveness, burden of illness, healthcare resource utilization) to contextualize clinical benefit in hematologic oncology. Ensure economic and outcomes evidence is scientifically rigorous, clinically meaningful, and suitable for external scientific exchange under Medical Affairs standards. Collaborate cross functionally to ensure consistency of value messaging while maintaining Medical Affairs independence and compliance. Scientific Communication & External Engagement Lead or support development of HEOR related abstracts, posters, manuscripts, and congress submissions in hematologic oncology. Serve as a Medical Affairs HEOR subject matter expert to support MSL training, scientific platforms, and field medical needs. Support compliant scientific exchange with external experts, cooperative groups, and other stakeholders on outcomes and RWE. Cross Functional & Vendor Collaboration Work closely with Medical Directors, Clinical Development, Market Access, and Regulatory colleagues to ensure integrated and nonpromotional evidence planning. Manage external vendors and academic collaborators to ensure high quality execution of HEOR studies. Oversee timelines, deliverables, and budgets for assigned HEOR initiatives. Required Qualifications Advanced degrees (PhD, DrPH, ScD, MD, PharmD), with experience in health economics, outcomes research, epidemiology, public health, health services research, or related fields. 4-6+ years of experience in HEOR, outcomes research, or RWE within pharmaceutical, biotech, consulting, or academic environments. Candidates with advanced scientific degrees may be considered with fewer years of industry experience. First-hand experience executing site-based non-interventional studies, systematic literature reviews, claims / administrative database analysis, patient-reported outcomes and health economic modeling. Ability to translate complex data into clinically relevant insights for scientific audiences. Experience with scientific publications and congress presentations. Strong cross functional collaboration and project management skills. High standards for scientific rigor, compliance, and Medical Affairs independence. Preferred Qualifications Experience in Global dossier preparation (preferably EU region). Prior experience in hematologic oncology or closely related oncology settings is strongly preferred. Demonstrated experience supporting Medical Affairs or clinical focused evidence generation. Experience supporting cross-functional internal stakeholders. Familiarity with treatment landscape of treatment and evolving standards of care in hematologic malignancies. Strong entrepreneurial spirit who can work independently and proactively. Experience working across global or regional Medical Affairs organizations.

Responsibilities

This role involves leading the development and execution of Medical Affairs aligned Health Economics and Outcomes Research (HEOR) and Real-World Evidence (RWE) data generation for hematologic oncology assets across prelaunch and postlaunch phases. The Associate Director will also oversee the design and interpretation of health economic analyses to contextualize clinical benefit and support scientific communication.