Key Responsibilities

• Define and execute the long-term scientific roadmap and R&D objectives
• Lead preclinical research efforts and ensure alignment with corporate timelines
• Direct the finalization of nonclinical reports and regulatory filings
• Manage scientific partnerships and academic collaborations
• Oversee scientific due diligence for licensing and M&A activities
• Represent the organization to global scientific and regulatory agencies

Essential

• Minimum of 15 years of biopharmaceutical industry experience
• Extensive background in immuno-oncology full-cycle drug development
• Proven track record from early discovery through first-in-human clinical trials
• Significant senior-level leadership and management experience
• Direct experience in oncology and tumor biology
• Expertise in writing and reviewing regulatory documents and nonclinical study reports
• Experience in intellectual property evaluation and scientific due diligence

Preferred

• Experience with monoclonal antibodies, bispecific antibodies, and antibody-drug conjugates (ADCs)
• History of working in both small-scale biotech and large pharmaceutical environments
• Established network within academic and scientific research institutions
• Experience managing both internal teams and external CROs

Key Skills