Executive Director, Clinical Development - Hematology Oncology

Location: Wilmington, Delaware, United States, or Morges, Switzerland

Company

hirify.global is a global, science-driven biopharmaceutical company developing targeted and immune-based therapies in hematology, oncology, and immunology.

What you will do

• Provide medical and scientific leadership to cross-functional clinical development, biostatistics, pharmacokinetics, pharmacovigilance, regulatory, and clinical operations teams.
• Guide the strategy, design, and execution of clinical development programs for anti-cancer agents across Phase I–III.
• Lead interactions with global regulatory authorities, including the FDA and EMA, and contribute to INDs, NDAs, and other regulatory submissions.
• Oversee protocols, informed consent forms, clinical study reports, investigator materials, publications, and development plans.
• Partner with discovery, translational, Medical Affairs, CRO, academic, and strategic partners to advance compounds and support global trials, launches, and lifecycle management.
• Identify and mitigate clinical and program risks while providing medical oversight for investigator-sponsored trials and representing the organization at scientific forums.

Requirements

• M.D. or D.O. degree required.
• Board certification or eligibility in Oncology strongly preferred.
• At least 3–5 years of oncology drug development experience in the biopharmaceutical industry or equivalent academic clinical research experience.
• Experience contributing to clinical development programs across multiple development phases.
• Strong understanding of oncology drug development, clinical trial design, data interpretation, and regulatory requirements.
• Excellent communication, organizational, prioritization, and cross-functional collaboration skills in a fast-paced matrixed environment.

Culture & Benefits

• Work within a science-driven biopharmaceutical environment focused on hematology, oncology, and immunology.
• Collaborate with global regulatory authorities, external research partners, and multidisciplinary internal teams.
• Contribute to early development, evidence generation, product launches, and lifecycle management.