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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.

Lead the hematology marketing team to develop and execute pre-launch and launch brand strategies and promotional plans for HCP and patient audiences; drive launch readiness and cross-functional alignment; manage and mentor direct report(s); support lifecycle management, publications, and KOL engagement.

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.

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