Reference Number: JO-1901-422312
Global Medical Director – Neurology
Rate: Negotiable
Job Type: Permanent
Location: Jersey City

Are you committed to helping patients defeat their cancer through your passion for oncology drug development? CPL Physicians is working with a clinical-stage biotech company that is pioneering breakthrough solutions to advance the next generation of immuno-oncology treatments for hematological malignancies and solid tumors. The well-funded company is seeking a Medical Director to lead the engagement of new and complementary phagocytic pathways that enhance anti-tumor efficacy and selectivity. Reporting to the Vice President, Clinical Development, the successful candidate is responsible for providing clinical leadership in the definition of clinical development strategies, as well as the design, execution, and analysis of clinical studies.
Location: Menlo Park, CA

• Leads/participates in cross-functional hematology and oncology drug development matrix teams
• Lead the formulation of clinical development plans; responsible for the design of protocols and conduct of data review, analysis, and interpretation
• Functions in the role of medical monitor, providing medical oversight of multiple clinical studies and guidance on scientific, clinical and safety monitoring issues
• Primary clinical author of regulatory documents (IB, DSUR, annual reports, IND sections, CSR)
• Interface with US/international regulatory authorities
• Leads/participates in clinical and translational data review and analysis
• Serves as a medical/scientific expert to drug discovery teams; contributes to selection of discovery compounds, development of clinical strategy and transition of compounds into early phase development
• Builds relationships with thought leaders and principal investigators for input on disease areas in oncology and design of clinical programs and interacts with key opinion leaders
• Serves as scientific and medical expert at advisory boards and public forums

Education & Experience:
• MD required; board eligible or certified in hematology/oncology, with strong scientific background
• Experience/training in treatment of hematological malignancies is essential; experience in bone marrow transplantation is a plus
• 2+ years biopharma industry experience in oncology clinical development preferred
• Translational or clinical trials experience in immuno-oncology is a plus
• In depth knowledge of the drug development process and oversight of clinical trials
• Experience in filing US INDs and/or BLA/NDAs is a plus
• Passionate about oncology drug development and working in an innovative therapeutic field

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