Medical Director, Oncology Clinical Development (Solid Tumors)

📋 Description

• Manages the design and implementation of study protocols for a clinical development program in
• Oversees project-related education of investigators, study site personnel, and AbbVie study staff
• Has responsibility for oversight of clinical studies, monitoring overall study integrity, and
• Along with Clinical Operations, is responsible for oversight of study enrollment and overall
• Responsible for assessment and reporting of serious adverse events per corporate policy and
• Contributes to design, analysis, interpretation, and reporting of scientific content of protocols

🎯 Requirements

• Medical Doctor (M.D), Doctor of Osteopathy (D.O.), or non-US equivalent of M.D. degree with
• Completion of a residency program strongly preferred
• Completion of a subspecialty fellowship is desirable
• Ability to run a clinical research study with appropriate supervision
• Strong desire to collaborate in a cross-functional setting
• Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred

🎁 Benefits

• Paid time off (vacation, holidays, sick)
• Medical/dental/vision insurance and 401(k) to eligible employees
• Eligibility to participate in long-term incentive programs
• Base pay range of $192,500 to $327,000 per year, depending on geographic location and other factors