Executive Oncology Clinical Development Director

AbbVie; Massachusetts; On-site; USD 180,000 - 300,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k) plan

Long-term incentive programs

Job summary

AbbVie is seeking an experienced leader to direct clinical development programs, overseeing study design, data interpretation, and regulatory submissions. You will lead cross-functional teams across Medical Affairs, Regulatory, and Clinical Operations to advance therapeutic programs.

The role requires MD or DO with extensive clinical trial experience and proven ability to manage complex programs independently, ensuring compliance and data integrity across global studies.

Qualifications

• MD/DO or equivalent with relevant therapeutic specialty.
• At least 5 years (7 preferred) of clinical trial experience.
• Ability to lead complex clinical programs independently.

Responsibilities

• Lead design, analysis, interpretation, and reporting of clinical study data and regulatory submissions.
• Oversee study teams, timelines, enrollment, and data safety reporting.
• Coordinate cross-functional teams across Clinical Development, Medical Affairs, and Regulatory.
• Represent AbbVie in clinical development discussions and external meetings.

Skills

Clinical trial leadership

Cross-functional leadership

Regulatory knowledge

English communication

Independent program management

Education

MD or DO degree

Job description

AbbVie is seeking an experienced leader to direct clinical development programs, overseeing study design, data interpretation, and regulatory submissions. You will lead cross-functional teams across Medical Affairs, Regulatory, and Clinical Operations to advance therapeutic programs.

The role requires MD or DO with extensive clinical trial experience and proven ability to manage complex programs independently, ensuring compliance and data integrity across global studies.