Clinical Pharmacology Associate Director

Job Summary

Leading the development and execution of clinical biomarker strategies, the full-time Associate Director, Clinical Pharmacology will focus on identifying, validating, and implementing biomarker testing solutions for chronic myeloid leukemia (CML) in a fully remote capacity.

Key Responsibilities

• Develop and execute clinical biomarker strategies for CML and other oncology programs
• Evaluate biomarker testing solutions from CROs and clinical laboratories, ensuring compliance with regulatory standards
• Establish and manage partnerships with external laboratories for the development and validation of biomarker assays

Required Qualifications

• An MD, PhD, or Pharm D in a relevant discipline with industry experience; M.S. or B.S. with substantial experience may be considered
• 8+ years of experience with an advanced degree or 15+ years with a M.S. or B.S. in pharmaceutical, biotechnology, or clinical laboratory settings
• Significant experience in developing and implementing biomarker assays, particularly in oncology or hematology
• Demonstrated expertise with molecular testing for hematologic malignancies, including BCR::ABL1 mutation testing
• Familiarity with regulatory submissions and interactions with health authorities such as the FDA or EMA