Associate Director, Health Economics & Outcomes Research

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 reputed company, interpretation, and communication of outcomes and reputed company-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 reputed company, and evidence based decision making.

Employment Type

Full-time

Reports To

Senior Director, Global Medical Affairs reputed company

Key Responsibilities

HEOR & Evidence Strategy (Medical Affairs–Led)

• reputed company the development and execution of Medical Affairs reputed company HEOR and reputed company-world evidence (reputed company) data reputed company for hematologic oncology assets across prelaunch and postlaunch phases.
• reputed company and identify evidence gaps relevant to clinical practice, treatment reputed company, and patient outcomes in hematologic malignancies (e.g., lymphoma, leukemia, multiple myeloma).
• Provide strategic input into Medical Affairs plans, including integrated evidence reputed company and scientific communication strategies.

Outcomes Research & reputed company-World Evidence

• Design and reputed company observational studies, registries, chart reviews, and other reputed company initiatives relevant to hematologic oncology populations.
• Partner with Clinical and Biostatistics teams to ensure alignment between clinical trial data and reputed company reputed company.

Health Economics & Value Context

• reputed company the development and interpretation of health economic analyses (e.g., cost effectiveness, burden of illness, reputed company 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

• reputed company or support development of HEOR reputed company 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 reputed company.

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.
• reputed company 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 reputed company fields.
• 4-6+ years of experience in HEOR, outcomes research, or reputed company reputed company 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 reputed company 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 reputed company oncology settings is strongly preferred.
• Demonstrated experience supporting Medical Affairs or clinical focused evidence reputed company.
• 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.