Director, HEOR – Contract

🕒 vor 1 Monat

🏄 California – Remote

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💵 $75 - $130 / Stunde

⏳ Vertrag

🔴 Experte

👔 Direktor

🦅 H1B-Visum-Sponsor

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👻 Geisterscore 0%

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🗣️🇺🇸🇬🇧 Englisch erforderlich

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Logo of Adverum Biotechnologies

Adverum Biotechnologies

51 - 200 Mitarbeiter

Gegründet 2013

🏥 Gesundheitswesen

🧬 Biotechnologie

💊 Pharmazie

💰 €217.000.000 Post-IPO Equity im 2020-08

Healthcare • Biotechnology • Pharmaceuticals

Adverum Biotechnologies ist ein Unternehmen, das sich auf die Entwicklung von Gentherapien zur Behandlung schwerwiegender Augenerkrankungen konzentriert. Ihr Ziel ist es, die Gentherapie als neuen Standard der Versorgung zu etablieren, insbesondere bei der Behandlung von Erkrankungen wie der feuchten altersbedingten Makuladegeneration (feuchte AMD), einer der weltweit führenden Ursachen für Erblindung. Das Unternehmen entwickelt seine experimentelle Gentherapie Ixo-vec, die eine langanhaltende Behandlung durch eine einzige ambulante Verabreichung bieten soll, was die derzeitige Praxis häufiger und schmerzhafter Augeninjektionen ersetzen könnte. Durch die Nutzung ihrer proprietären adeno-assoziierten Virus (AAV) Vektor-Plattform möchte Adverum den Versorgungsstandard verändern, den Zugang zur Behandlung verbessern und einen signifikanten gesellschaftlichen Einfluss erzielen, indem sie das Sehvermögen wiederherstellen und Erblindung verhindern.

Beschreibung

• Lead the development and execution of evidence generation strategies across marketed and pipeline assets, indications, and geographies • Oversee the design and conduct of multiple programs and communicate findings and strategic impact to internal and external audiences • Serve as HEOR strategy lead with cross-functional brand teams • Determine global development strategy for new or marketed products and contribute to Therapeutic Area Long Range Plan and Portfolio Planning • Drive design and execution of HEOR programs supporting pipeline and on-market products while meeting ethical, scientific, regulatory, commercial, and quality requirements • Develop and execute post-marketing product life cycle and labeling strategies across the therapeutic area portfolio • Ensure scientific and communication excellence of agreed data elements • Deliver the HEOR book of work from strategy development through content pull-through • Partner with HEOR COE functions to represent a comprehensive HEOR voice in cross-functional meetings • Engage senior leaders and demonstrate executive presence in cross-functional settings

🎯 Anforderungen

• Advanced degree: MD, PharmD, or MS • Minimum of ten years of working experience with a Master’s, or seven years with a PhD; fellowship experience may be included • Professional training in a health field is a plus • Ophthalmology/Retina experience is required • Experience leading complex products and/or clinical development supporting pipeline development and on-market product support • Pharmaceutical industry experience preferred • Ability to work in uncharted territory with few established guidelines or procedures • Ability to direct compliance with complex governmental rules and regulations • Ability to develop creative and effective solutions to priority conflicts, resource constraints, and other problems across multiple programs • Extensive knowledge of the global regulatory, HTA, and PR&A landscape • Understanding of development-related functions across all phases of drug development • Proven leadership skills in a cross-functional global team environment • Ability to interact with senior management globally and act as HEOR project/group champion and spokesperson • High goal orientation, self-starter mindset, and strong desire to achieve commercial success • Ability to lead cross-functional teams and manage scientific personnel in clinical research

🏖️ Vorteile

• Hourly compensation of $75.00–$130.00 USD per hour • Compensation and benefits provided in accordance with specific state requirements • Paid sick leave accrual • Opportunity to contribute to meaningful work within gene therapy and ophthalmology care

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