Senior Director, Clinical Science, Gynecologic Oncology (Oncology)

Location: Hybrid; primary location in Rahway, New Jersey, USA. The role is available in four locations and is limited to residents of the United States, Canada, and Puerto Rico. No relocation; 10% travel required.

Salary: $210,400–$331,100 annual base salary for the primary location, plus eligible annual bonus and long-term incentive.

Company

hirify.global is a pharmaceutical and biotechnology company developing medicines through clinical research and drug development.

What you will do

• Lead Clinical Science strategy across multiple gynecologic oncology studies, programs, and assets.
• Apply expertise in gynecologic cancers, disease biology, treatment landscapes, clinical endpoints, and oncology data interpretation to study planning and development decisions.
• Standardize medical data review practices, scientific approaches, deliverables, and endpoint interpretation across the portfolio.
• Contribute to protocol development, amendments, study design, eligibility criteria, biomarker strategy, regulatory submissions, safety reviews, and health authority interactions.
• Present scientific assessments and cross-study insights in portfolio, governance, senior leadership, and cross-functional forums.
• Manage, coach, and develop Directors, Principal Scientists, and Clinical Scientists while leading through a matrix environment.

Requirements

• Advanced scientific or healthcare degree, such as PhD or PharmD, is required, with 8+ years of pharmaceutical, clinical drug development, and/or medical field experience preferred; alternatively, a master’s degree preferably in life sciences with 12+ years of relevant experience, or a bachelor’s degree preferably in life sciences with 15+ years of relevant experience.
• Significant experience in Clinical Development, Clinical Science, clinical drug development, or a related pharmaceutical or biotechnology function.
• Demonstrated Clinical Science leadership across multiple studies, programs, or assets.
• Deep therapeutic expertise in gynecologic cancers, including disease biology, current and emerging treatment landscapes, clinically relevant endpoints, and development strategy considerations.
• Strong understanding of clinical trial design, clinical development strategy, clinical data review, and oncology data interpretation.
• Experience contributing to disease-area strategy, portfolio discussions, or cross-program planning.
• Experience contributing to regulatory submissions, safety reviews, or health authority interactions.
• Experience working effectively in cross-functional teams within a matrix environment and integrating information across studies and programs.
• Excellent communication, influence, executive presentation, people leadership, management, coaching, and scientific staff development skills.

Nice to have

• Experience with visual analytics, centralized data review, AI-enabled workflows, or other technologies that improve Clinical Science quality and efficiency.

Culture & Benefits

• Hybrid work arrangement with a collaborative, inclusive, matrix-based environment.
• Medical, dental, vision, and other insurance benefits for employees and families.
• Retirement benefits including a 401(k), paid holidays, vacation, compassionate leave, and sick days.
• Culture focused on accountability, continuous learning, inclusion, strong performance, and respectful challenge.