Senior/Executive Medical Director, Clinical Development (Hematology/Oncology)

Location: San Carlos, California, or remote within the United States. Must be permitted to work in the United States. Travel up to 25% may be required.

Base pay: $275,000–$325,000 per year, depending on work location, skills, experience, and education or training.

Company

hirify.global is a privately held, clinical-stage biopharmaceutical company developing antibody therapeutics for cancer, autoimmune disorders, and other serious diseases.

What you will do

• Contribute to clinical development plans and lead the design and implementation of hematology/oncology clinical studies.
• Serve as clinical lead and medical monitor for one or more clinical studies.
• Develop and review protocols, investigator brochures, clinical study reports, regulatory documents, registration dossiers, and publications.
• Review and interpret ongoing safety data in collaboration with pharmacovigilance.
• Conduct investigator meetings and lead site initiation visits with clinical investigators.
• Translate research and nonclinical findings into clinical development opportunities while collaborating with internal and external stakeholders.

Requirements

• M.D. degree with board certification or specialization in Hematology strongly preferred.
• At least 5 years of industry experience or relevant drug development experience managing and executing Phase I–III trials.
• Experience serving as medical monitor for early- and late-stage hematology/oncology clinical trials.
• Experience designing, implementing, and conducting clinical trials, with knowledge of the hematology/oncology competitive and regulatory landscape.
• Familiarity with U.S. and international regulatory frameworks, including CFR21, ICH, and GCP, as well as U.S. and EU drug development regulations.
• Must be permitted to work in the United States and willing to travel up to 25%.

Culture & Benefits

• Competitive cash compensation and equity incentive awards.
• Employer-sponsored benefit offerings.
• Cross-functional collaboration across Research, Translational Sciences, Clinical Operations, Regulatory, Patient Safety, Medical Affairs, and Commercial.
• Fast-paced environment requiring independent judgment, adaptability, and flexible prioritization.
• Opportunities to support strategic corporate initiatives and interact with investigators, medical experts, advisory boards, and patient advocacy groups.

Hiring process

• Submit a resume and cover letter to careers@drenbio.com.