Associate Scientific Director, Oncology Early Development

📋 Description

• Oversees design, planning and interpretation of clinical trials.
• Participates in cross‑functional teams to deliver clinical data.
• Design and implement Phase 1 study protocols under supervision.
• Oversees study enrollment and timelines with Clinical Operations.
• Contributes to protocols, CSRs and regulatory submissions.
• Maintains regulatory compliance and quality standards.

🎯 Requirements

• Bachelors in sciences; advanced degree required.
• Ability to provide input and direction under supervision.
• Strong cross‑functional collaboration skills.
• Clinical trial experience in pharma/academic settings required.
• Knowledge of trial methodology and regulatory requirements.
• Excellent oral and written English communication.

🎁 Benefits

• Comprehensive benefits package including PTO and health insurance.
• Eligibility to participate in long‑term incentive programs.
• Equal opportunity employer; committed to integrity and inclusion.