Associate Scientific Director, Oncology Early Development

📋 Description

• Oversees direction, planning, execution and interpretation of clinical trials or research
• Participates in cross-functional teams to generate and deliver high-quality clinical data
• Manages design and implementation of first-in-human (Phase 1) study protocols for a development
• Oversees study enrollment and overall timelines for key deliverables with Clinical Operations.
• Contributes to design, analysis, interpretation and reporting of scientific content for protocols
• May contribute to development of a cross-functionally-aligned Clinical Development Plan.

🎯 Requirements

• Bachelors degree in the sciences; advanced degree (MS, PhD) required.
• Ability to provide input and direction to clinical research under supervision.
• Strong collaboration skills in a cross-functional setting.
• Clinical trial experience in pharma/academia or equivalent is required.
• Knowledge of trial methodology, regulatory and compliance requirements; experience designing study
• Ability to interact with internal and external stakeholders to support global strategy.

🎁 Benefits

• AbbVie offers a comprehensive benefits package including paid time off, medical/dental/vision
• Eligible to participate in long-term incentive programs.