Jobs at Deciphera Pharmaceuticals

The Director, Product Counsel provides legal counsel for Commercial, Medical Affairs, and Patient Support teams regarding FDA regulations and compliance, advising on launch strategies and overseeing promotional activities.

The Senior Manager, Cybersecurity & Compliance will lead the design and management of cybersecurity and compliance programs, ensuring alignment with industry standards.

The Executive Director leads Deciphera's global Total Rewards strategy, overseeing compensation, benefits, HR technology, and operations while ensuring alignment with business priorities and operational excellence.

The Senior Director of Talent, Learning & Organizational Development leads the development of talent strategies across the employee lifecycle, emphasizing performance management and leadership development, enhancing organizational effectiveness, and fostering a high-performance culture.

The Associate Director, Pharmacovigilance Scientist oversees safety data analyses, signal management, and regulatory submissions, leading strategic initiatives and mentoring junior staff.

The Senior Director, Legal Counsel will lead the Contracts Team, provide legal advice on agreements, and oversee legal operations and strategic initiatives across the organization.

The Director oversees Market Access strategies, focusing on pricing, contracting, and reimbursement through advanced analytics. Responsibilities include stakeholder alignment, financial modeling, and cross-functional team collaboration to enhance patient access and support business growth.

The Director of New Product Planning will lead commercial strategy for clinical-stage assets, collaborating cross-functionally to optimize development and market entry strategies while providing competitive intelligence leadership.

The Associate Director provides leadership and strategic direction for drug development programs, ensuring effective program management and communication across teams.

The role involves leading the IT compliance and CSV/CSA framework, ensuring regulatory compliance, managing audits and inspections, overseeing validation activities, and partnering with various stakeholders.

Lead field operations for a hematology commercial launch: define strategy, manage CRM/roster/reporting platforms, oversee territory design and onboarding, ensure FDA/OIG compliance, deliver dashboards and KPIs, drive continuous improvement, and partner cross-functionally to enable field success.

Lead statistical strategy and oversight for multiple clinical studies across all phases. Design studies, author protocols and SAPs, oversee interim/final analyses, ensure reproducible outputs with programming teams/CROs, support regulatory submissions and inspections, manage external vendors, mentor junior statisticians, and contribute to publications and presentations.

The Vice President, US Market Access develops and executes market access strategies for rare oncology therapies, leading a team to optimize access, reimbursement, and collaborate across commercial functions.