Director, Oncology Clinical Affairs – MD

atCorcept TherapeuticsRemoteUS flagUnited StatesFull-timeDirectorLead$209.1k – $307.6k/year

Posted 19 hours ago

This is a fully remote position, open to applicants in United States.

πŸ“‹ Description

β€’ Act as a senior clinical associate within the Oncology division, reporting directly to the President of Oncology.

β€’ Facilitate high-level clinical and scientific interactions with external oncology specialists, serving as a liaison between Clinical Development, Medical Affairs, Commercial, Market Access, HEOR, Pharmacovigilance, and Regulatory teams.

β€’ Assist in shaping and implementing the introduction of Lifyorli into clinical practice, chiefly in the U.S. market.

β€’ Aid in executing the medical affairs strategy and act as the primary contact for practitioners seeking peer-to-peer engagements.

β€’ Support payer-facing engagement by utilizing clinical guidelines.

β€’ Address medical priorities related to product adoption and long-term integration into clinical settings.

β€’ Provide clinical and medical/scientific expertise for medical affairs priorities, tactical planning, internal training, advisory boards, congress activities, and cross-functional initiatives.

β€’ Identify unmet medical needs and convert scientific insights into actionable clinical guidance.

β€’ Lead peer-to-peer scientific discussions with oncology experts, KOLs, clinical researchers, academic institutions, and external medical stakeholders.

β€’ Engage physicians and oncology specialists through advisory boards, congress interactions, speaker preparation, and insight-gathering initiatives.

β€’ Represent Corcept at medical conferences and other external events.

β€’ Offer clinical input into post-approval evidence generation, including RWE, ISS, registries, and additional data-generation activities.

β€’ Review ISS proposals and collaborate on program design, prioritization, and governance.

β€’ Assess clinical trial outcomes, post-marketing evidence, medical literature, and emerging oncology trends.

β€’ Ensure accurate, balanced, and compliant scientific, educational, medical information, and promotional review materials.

β€’ Interpret and influence updates to clinical guidelines and treatment pathways, including those from NCCN and ASCO.

β€’ Convey guideline and pathway alterations into clinical and business implications for internal teams.

β€’ Collaborate with Market Access and HEOR on payer value propositions, outcomes, comparative effectiveness, and economic value.

β€’ Participate in payer-facing discussions necessitating deep clinical expertise.

β€’ Develop and communicate safety-related clinical guidance alongside Pharmacovigilance, Clinical Development, and Medical Affairs.

β€’ Transform safety data into clinician-facing recommendations, monitoring strategies, risk mitigation tactics, and adverse event management protocols.

β€’ Contribute to supportive care guidance and safety-related external communications.


⛳️ Requirements

β€’ MD degree is required.

β€’ Experience in Oncology is required; gynecologic oncology experience is preferred.

β€’ 3-5+ years of relevant oncology practice experience, including fellowship.

β€’ Proven experience in engaging oncology experts, interpreting clinical evidence, and translating complex data into clear scientific and clinical communications.

β€’ Demonstrated capability to evaluate scientific data, clinical literature, evolving treatment pathways, and oncology practice trends, applying insights to medical, launch, market access, and evidence-generation activities.

β€’ Knowledge of the U.S. healthcare landscape, health technology assessment (HTA) considerations, payer evidence needs, and the pharmaceutical/biotechnology sector.

β€’ Strong oral, written, and presentation skills, with the capability to clearly communicate complex clinical concepts to both internal and external audiences.

β€’ Collaborative and cross-functional leadership style, demonstrating sound judgment and scientific rigor.

β€’ Ability to function effectively in a launch-focused, dynamic environment.

β€’ Willingness to travel 25-30% or as needed.

β€’ Applicants must be currently authorized to work in the United States on a full-time basis.


🏝️ Benefits

β€’ Comprehensive health insurance.

β€’ Retirement savings plan with company match.

β€’ Opportunity for professional development and continuing education.

β€’ Flexible work arrangements.

β€’ Generous paid time off policy.

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