Director, Oncology Clinical Affairs – MD

🕒 Novembro 3

🇺🇸 Estados Unidos – Remoto (EUA)

💵 $209.100 - $307.600 / ano

⏰ Tempo Integral

🔴 Especialista

👔 Diretor

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Corcept Therapeutics

SiteLinkedInTodas as Vagas

201 - 500 funcionários

Fundada em 1997

🏥 Saúde

🧬 Biotecnologia

💊 Farmacêutico

💰 $525.300 Post-IPO Equity em 2012-04

Healthcare • Biotechnology • Pharmaceuticals

A Corcept Therapeutics é uma empresa biofarmacêutica focada em liberar o potencial da modulação do cortisol para revolucionar o tratamento de doenças graves. A empresa é dedicada a entender e modular a atividade do cortisol no receptor de glicocorticoides para desenvolver tratamentos inovadores para distúrbios severos. Com mais de 30 estudos em andamento, a Corcept está construindo uma base científica para oferecer novas abordagens em áreas como endocrinologia, oncologia, metabolismo e neurologia. A empresa busca trazer terapias inovadoras aos pacientes explorando novas possibilidades na ciência da modulação do cortisol.

Descrição

• Serve as a senior clinical associate within Oncology, reporting to the President of Oncology • Lead high-level clinical and scientific engagement with external oncology experts and serve as a bridge between Clinical Development, Medical Affairs, Commercial, Market Access, HEOR, Pharmacovigilance, and Regulatory partners • Help shape and execute the introduction of Lifyorli in clinical practice, primarily in the U.S. market • Support execution of medical affairs strategy and serve as the primary contact for practitioners seeking peer-to-peer interactions • Support payer-facing engagement leveraging clinical guidelines • Support medical priorities related to product adoption and long-term integration into clinical practice • Provide clinical and medical/scientific expertise for medical affairs priorities, tactical planning, internal training, advisory boards, congress activities, and cross-functional initiatives • Identify unmet medical needs and translate scientific insights into practical clinical guidance • Lead peer-to-peer scientific interactions with oncology experts, KOLs, clinical researchers, academic centers, and external medical stakeholders • Engage physicians and oncology experts through advisory boards, congress interactions, speaker preparation, and insight-gathering activities • Represent Corcept at medical conferences and external events • Provide clinical input to post-approval evidence generation, including RWE, ISS, registries, and other data-generation activities • Review ISS proposals and collaborate on program design, prioritization, and governance • Evaluate clinical trial results, post-marketing evidence, medical literature, and emerging oncology trends • Support accurate, balanced, and compliant scientific, educational, medical information, and promotional review materials • Interpret and influence clinical guideline updates and treatment pathways, including NCCN and ASCO • Translate guideline and pathway changes into clinical and business implications for internal teams • Partner with Market Access and HEOR on payer value propositions, outcomes, comparative effectiveness, and economic value • Participate in payer-facing discussions requiring deep clinical expertise • Develop and communicate safety-related clinical guidance with Pharmacovigilance, Clinical Development, and Medical Affairs • Translate safety data into clinician-facing recommendations, monitoring strategies, risk mitigation approaches, and adverse event management algorithms • Contribute to supportive care guidance and safety-related external communications

🎯 Requisitos

• MD required • Oncology experience required; gynecologic oncology experience preferred • 3-5+ years of relevant oncology practice, including fellowship • Experience engaging oncology experts, interpreting clinical evidence, and translating complex data into clear scientific and clinical communications • Demonstrated ability to evaluate scientific data, clinical literature, evolving treatment pathways, and oncology practice trends and apply insights to medical, launch, market access, and evidence-generation activities • Understanding of the U.S. healthcare environment, health technology assessment (HTA) considerations, payer evidence needs, and the pharmaceutical/biotechnology industry • Strong oral, written, and presentation skills, with the ability to communicate complex clinical concepts clearly to internal and external audiences • Collaborative, cross-functional leadership style with sound judgment and scientific rigor • Ability to operate effectively in a launch-focused, evolving environment • Ability to travel 25-30% or as needed • Applicants must be currently authorized to work in the United States on a full-time basis

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