
Director, Oncology Clinical Affairs β MD
Posted 19 hours ago

Posted 19 hours ago
This is a fully remote position, open to applicants in United States.
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.
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.
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.
Jazz Pharmaceuticals
Ulteig
Real Chemistry
ERM
Get handpicked remote jobs straight to your inbox weekly.