Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com.
Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.
Brief Team/department Description
- The Manager, Medical Materials, is responsible for the strategic development, execution, and lifecycle management of high-quality medical education and scientific materials that support Medical Affairs objectives. Reporting to the Director, Medical Education, this role ensures materials are scientifically accurate, compliant, and aligned with product strategy across the lifecycle. The Manager will partner cross-functionally with Medical Affairs, Regulatory, Legal, Compliance, Commercial, and external vendors to deliver effective, patient- and HCP-focused educational assets.
Principle Responsibilities
- Lead development and maintenance of medical education and scientific materials, including core slide decks, FAQs, scientific response documents, training materials, and disease-state education.
- Translate complex clinical and scientific data into clear, balanced, and compliant medical content for internal and external audiences.
- Support product launches and lifecycle management through creation of foundational medical materials.
- Partner with PMRC/SRC stakeholders to facilitate timely review and approval of materials.
- Collaborate closely with Medical Affairs, Regulatory Affairs, Legal, Compliance, Commercial, and Field Medical teams.
- Serve as a medical content subject-matter partner while maintaining appropriate separation between promotional and non-promotional activities.
- Manage external agencies and vendors supporting medical content development.
- Oversee timelines, budgets, and quality of deliverables.
- Support training of internal stakeholders in the use of medical materials and scientific narratives.
- Identify opportunities to enhance content quality, efficiency, and alignment with evolving best practices.
Qualifications And Education Requirements
This section should include relevant qualifications and education requirements.
- 5+ years of experience in Medical Affairs, medical education, medical communications, or scientific content development within pharmaceutical or biotechnology organizations
- Bachelor’s degree required; advanced degree (PharmD, PhD, MD, or MS) in life sciences or related field preferred.
By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.
