Senior Medical Director, Oncology Early Development

📋 Description

• Lead direction, planning, execution, and interpretation of early phase clinical trials or research
• Guide cross-functional teams to generate and disseminate high-quality clinical data.
• Oversee design and implementation of clinical development programs and study timelines.
• Ensure regulatory compliance, GCP standards, and safety monitoring across studies.
• Provide in-house clinical expertise and coordinate translational strategies with stakeholders.
• Participate in regulatory discussions and contribute to Clinical Development Plans.

🎯 Requirements

• Medical Doctor (M.D.), D.O., or non-US equivalent with oncology subspecialty desirable.
• At least 3 years of clinical trial experience; at least 2 years in pharmaceutical industry.
• Proven ability to lead cross-functional global teams and complex programs.
• Strong communication skills in English; experience with PK/PD modelling valued.
• Experience in thoracic malignancies and/or T-cell engagers preferred.
• Knowledge of regulatory, safety, and development of clinical strategy and protocols.

🎁 Benefits

• Competitive compensation package with comprehensive benefits.
• Equal Opportunity Employer; support for work-life balance and professional development.
• Long-term incentive programs eligibility.