Scientific Director I, Oncology Clinical Development

📋 Description

• With supervision, directs clinical trials and research activities.
• Participates in cross-functional teams to deliver high-quality data.
• Manages study protocols for a clinical development program.
• Oversees safety and efficacy data review and timelines.
• Contributes to protocol design, reports and regulatory submissions.
• Stays current with regulatory requirements and GCP.

🎯 Requirements

• Bachelor's degree in sciences; MS/PhD preferred.
• Ability to provide input and direction with supervision.
• Strong collaboration in a cross-functional setting.
• Clinical trial experience in pharma or academia preferred.
• Knowledge of trial methodology and regulatory requirements.
• Excellent English communication, both oral and written.

🎁 Benefits

• Comprehensive benefits: PTO, medical/dental/vision, 401(k).
• Eligible for long-term incentive programs.
• AbbVie is an equal opportunity employer.