Executive Director, Product Development Team Leader, Clinical Research, Hematology - Lymphoma

Location: Hybrid, with positions available in Rahway, New Jersey; Boston, Massachusetts; or Upper Gwynedd, Pennsylvania, United States. The role is for US and Puerto Rico residents only and requires approximately 25% travel.

Salary: $310,900–$489,400 annual base salary for the primary Rahway location, plus annual bonus and long-term incentive eligibility.

Company

hirify.global develops and advances investigational and marketed medicines through clinical research and product development.

What you will do

• Plan and direct late-stage clinical research activities from Phase 2 through Phase 5, including strategy, protocol authoring, trial initiation, execution, monitoring, analysis, regulatory reporting, publications, and presentations.
• Lead cross-functional Product Development Teams and clinical subteams overseeing product strategy and execution.
• Evaluate preclinical and translational work, develop early clinical plans, and support Investigational New Drug applications.
• Analyze clinical findings to support safety and efficacy decisions, new drug applications, clinical study reports, and publications.
• Coordinate with commercialization, regulatory affairs, statistics, manufacturing, senior management, committees, investigators, and external research partners.
• Manage Clinical Directors and Senior Clinical Directors, maintain scientific expertise, and travel for clinical research projects and scientific meetings.

Requirements

• M.D. or M.D./Ph.D.
• Minimum of 3 years of clinical medicine experience.
• Minimum of 5 years of industry experience in drug development, with demonstrated success overseeing multiple studies and protocols through completion.
• Experience authoring regulatory documents and leading discussions with regulatory agencies.
• Demonstrated scientific scholarship and achievement, with a proven track record in clinical medicine and biomedical research.
• Outstanding interpersonal and collaborative skills, with the ability to function in a matrix environment.
• Excellent verbal, written, and presentation communication skills.
• Required expertise includes clinical development, clinical judgment, clinical medicine, clinical trial development, ethical standards, hematology, interdisciplinary problem solving, mentorship, program strategy, regulatory compliance, scientific leadership, senior program management, and strategic planning.

Nice to have

• Board certification or eligibility in oncology, hematology, or a related discipline.
• Lymphoma experience.
• Prior clinical research experience and a publication record.
• Product registration experience.

Culture & Benefits

• Hybrid work arrangement with first-shift daytime hours.
• 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.
• Inclusive environment focused on diverse perspectives, respectful challenge, and collective problem solving.
• Visa sponsorship is available.