Head, Global Oncology Medical Affairs, Clinical Trial Management, Resources, Operations & Governance (Oncology)

Location: Basking Ridge, New Jersey, United States. Full-time, office-based role with up to 20% travel.

Salary: USD 271,500–452,500 per year.

Company

hirify.global is a global pharmaceutical company developing innovative medicines, with a primary focus on oncology and additional work in cardiovascular, rare disease, and immune disorders.

What you will do

• Lead global oncology medical affairs clinical programs, including company-initiated studies, non-interventional studies, and expanded access programs.
• Oversee study planning, protocol development, clinical deliverables, timelines, budgets, quality plans, databases, and regulatory documentation.
• Lead multidisciplinary global study teams and coordinate with medical, operations, safety, regulatory, quality, legal, supply, and regional functions.
• Manage CROs, investigators, suppliers, outsourcing specifications, partner selection, performance, budgets, contracts, and payments.
• Oversee investigator-initiated and external collaborative research processes, approvals, tracking, documentation, and compliance.
• Develop clinical operations standards, tools, SOPs, knowledge-sharing practices, and corrective and preventive action plans.

Requirements

• Bachelor’s degree required; a life science or healthcare degree is preferred, and an advanced degree is an advantage.
• At least 10 years of related professional experience, including preferred experience in pharmaceutical clinical research.
• At least 4 years of people management and development experience, including global people management.
• Extensive knowledge of clinical development, regulatory requirements, and Good Clinical Practice.
• Experience leading global clinical trials, managing vendors and projects, improving clinical operations processes, and working in a cross-functional matrix environment.
• Medical or scientific knowledge of oncology and/or haematology, with strong leadership, organizational, interpersonal, analytical, and problem-solving skills.

Culture & Benefits

• Work within a global pharmaceutical organization with operations in more than 30 countries.
• Collaborate across global and regional medical affairs, clinical operations, research, regulatory, quality, safety, and supply functions.
• Support a patient-first, values-driven environment focused on integrity and innovation.
• Travel is expected for up to 20% of working time; the role otherwise has standard office-based physical demands.