Senior Medical Director, Oncology Clinical Development (Solid Tumors)

📋 Description

• Oversee design and implementation of clinical development programs.
• Monitor study integrity; interpret safety and efficacy data.
• Oversee study enrollment and timelines for key deliverables.
• Design, analyze, and report protocols and regulatory documents.
• Provide in-house clinical expertise; coordinate with internal stakeholders.
• Stay updated on literature and training; ensure regulatory compliance and GCP.

🎯 Requirements

• Medical Doctor (MD), DO, or non-US MD with relevant specialty.
• Residency completed; subspecialty fellowship desirable.
• At least 2 years clinical trial experience in pharma or academia.
• Ability to run a clinical research program of moderate complexity.
• Ability to lead cross-functional global teams.
• Knowledge of trial methodology and regulatory requirements.
• Excellent oral and written English communication.

🎁 Benefits

• Paid time off, medical/dental/vision insurance.
• 401(k) retirement plan with company match.
• Eligible for long-term incentive programs.
• AbbVie is an equal opportunity employer.