Jobs at Deciphera Pharmaceuticals

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.

Lead development and execution of an integrated omnichannel marketing plan for Romvimza, creating branded and disease-state materials, field and digital programs, managing agencies and budgets, and using analytics and market intelligence to measure and optimize marketing performance.

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 Senior Director, Program Lead is responsible for managing the strategy and execution of therapeutic assets in drug development, leading cross-functional teams, and ensuring effective communication with stakeholders.

Lead and execute integrated development strategies for early-to-late phase clinical and lifecycle management programs. Partner with Program Lead to manage cross-functional program teams, track KPIs, identify risks, facilitate meetings, ensure clear communication, and integrate sub-teams to deliver program objectives.

Lead PV scientist for assigned products performing signal detection/management, aggregate report and RMP authorship, literature surveillance, safety analyses for regulatory filings, inspection readiness, process improvements, and mentorship of 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.

Lead GMP Quality Assurance for clinical and commercial products, overseeing batch release, partner GMP oversight, investigations/CAPA/change control, audits/inspections, quality system improvements, validation/tech transfer support, and mentoring junior QA staff to ensure global regulatory compliance.