Director, Scientific Affairs – Bone & Endocrinology

🕒 Maio 6

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Mirum Pharmaceuticals, Inc.

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201 - 500 funcionários

Fundada em 2018

🧬 Biotecnologia

💊 Farmacêutico

Biotechnology • Pharmaceuticals

A Mirum Pharmaceuticals, Inc. é uma empresa biofarmacêutica dedicada ao desenvolvimento e entrega de terapias transformadoras para doenças raras. O foco científico da empresa está em áreas terapêuticas como colestase, erros inatos do metabolismo dos ácidos biliares e neurologia genética, com ênfase em suprir necessidades médicas não atendidas. O medicamento carro-chefe da Mirum, LIVMARLI, está disponível nos EUA e na UE, enquanto seu pipeline apresenta outros candidatos promissores, como o Volixibat, com o objetivo de mudar a trajetória das doenças raras. Movida pela paixão pelos pacientes, a Mirum Pharmaceuticals está comprometida em revitalizar comunidades afetadas por doenças raras através de descobertas científicas significativas e terapias baseadas em evidências.

Descrição

• Leading data generation plans to address evidence gaps in the bone and endocrinology areas. • Driving real-world evidence activities (e.g., phase IV studies, managed access programs, etc.) to inform regulatory, commercial and access requirements. • Supporting the analyses and dissemination of data from real-world registries and data repositories for the therapeutic area. • Overseeing secondary analyses of clinical trials data based on field insights and critical knowledge gaps. • Contributing to the overall strategic plan and developing data generation and dissemination activities that support the plan • Leading the development of scientific publications that support the overall Brand Plan and Medical Strategic Plan that are directed towards the diagnosis and management of the therapeutic area • Partnering with other functional teams to develop educational materials for different stakeholders (e.g., physicians, patients) that aid in the diagnosis and management of the therapeutic area • Educating appropriate internal teams on the therapeutic area • Identifying, gaining access to, and developing professional relationships with thought leaders and other healthcare professionals, active and potential study investigators, and professional organizations within their assigned geography • Engaging in scientific exchange in response to thought leader requests • Serving as a liaison between HCPs who express interest in conducting investigator-initiated research to facilitate review and consideration of research proposals • Collaborating with external scientists and clinicians on projects related to the diagnosis and management for the therapeutic area • Utilizing scientific resources to deliver impactful presentations to varying audiences and in a variety of different settings including (but not limited to) advisory boards and patient advocacy groups.

🎯 Requisitos

• Advanced science or clinical degree at Masters level or above (e.g. MD, DO, Pharm.D., PhD, NP, PA, MPH, MHS, or MS) • Minimum of 5 years of experience in medical affairs or clinical/scientific research and publications • Knowledge in rare disease • Background in clinical research including experience generating and analyzing data • Previous experience as author on scientific publications • Proven ability to write and edit content for scientific abstracts, posters, presentations, digital enhancements, and manuscripts aligned with scientific narrative and objectives • Ability to work collaboratively with external stakeholders and internal cross-functional team. • Understanding of statistical methods in clinical study design, survival and longitudinal analysis • Background in epidemiology and/or biostatistics to enable the identification of the appropriate analytic strategy to evaluate scientific questions • Able to analyze data with Excel or equivalent • Outstanding oral and written communication skills with the ability to communicate complex scientific concepts in a compelling and concise manner to various internal and external stakeholders • Excellent interpersonal communication skills, strong personal integrity, adept at networking, and possesses strong oral, written, and communication skills • Able to identify relevant literature to support scientific publications and strategy • Skilled in the development and interpretation of data tables and visualizations to support scientific communication • Well-versed using common tools in scientific publications including collaborative authoring through MS Word, PowerPoint and Excel • Excellent collaboration skills to be able to work with other internal functions, external collaborators, authors/reviewers to obtain feedback and incorporate information into a final product • Able to organize and prioritize tasks in order to maintain deadlines • Able to travel up to 30%

🏖️ Benefícios

• Equal Employment Opportunity (EEO) commitment • Compliance with Federal, State and Local laws