Lead Deciphera’s global pharmacovigilance strategy and organization, overseeing patient safety, benefit-risk evaluation, safety governance, surveillance, signal management, and risk management for investigational and marketed products. Ensure compliant, inspection-ready operations and scalable systems while advising executive leadership and partnering across functions and with health authorities.
The Medical Director will provide clinical development leadership for clinical-stage assets, serving as a medical monitor and overseeing clinical trial data review. They will also contribute to regulatory document authoring, strategy development, and cross-functional collaboration with internal and external stakeholders.
The Associate Director of Sales Operations leads the operational infrastructure for field-based commercial teams, including strategy, systems, and performance management. They are responsible for designing incentive compensation plans, managing CRM platforms, and ensuring data-driven decision-making across the organization.
The Medical Science Liaison will build and maintain peer-to-peer relationships with key opinion leaders and healthcare professionals to provide balanced, evidence-based information on therapies. They will also gather clinical insights, support research initiatives, and collaborate cross-functionally to inform medical strategy.
Lead and optimize field operations, including strategy, incentive compensation, territory and roster management, CRM systems, reporting, and launch readiness. Partner with commercial and cross-functional leaders to ensure compliant, data-driven field execution and continuously improve operational processes.
The Medical Science Liaison will serve as a field-based scientific expert, building peer-to-peer relationships with key opinion leaders and healthcare professionals in oncology. They will gather clinical insights, support research initiatives, and ensure scientific communications are accurate and strategically aligned with company goals.
The Medical Director will provide clinical development leadership for clinical-stage assets, serving as a medical monitor and overseeing clinical trial data review. They will also contribute to regulatory document authorship, strategic planning, and cross-functional collaboration with internal and external stakeholders.
The Vice President of Pharmacovigilance will lead global drug safety strategy, ensuring regulatory compliance and proactive benefit-risk assessment for all products. This executive will oversee safety governance, signal management, and the development of a high-performing safety organization.
The Vice President of Pharmacovigilance will lead global drug safety strategy, ensuring regulatory compliance and proactive benefit-risk assessment for all products. They will oversee safety governance, signal management, and the development of a high-performing organization while partnering across clinical and commercial functions.
Provide clinical development leadership for early and late-stage assets, serving as a medical monitor and authoring key regulatory documents. Foster collaboration across functions and manage relationships with key opinion leaders to advance product candidates.
