Associate Director, Health Economics & Outcomes Research

Secura Bio, Inc.

3d

About The Position

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.

Requirements

• 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.

Nice To Haves

• 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

• 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.
• 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.
• 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.
• 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.
• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree