Oncology Clinical Development Lead

BioSpace; North Chicago (IL); On-site; USD 250,000 - 360,000; Full time

Benefits offered by this job

Health insurance

401(k) plan

Paid time off

Job summary

AbbVie is seeking a senior medical director to lead multiple clinical development programs, guiding design, analysis, and reporting of pivotal studies. You will mentor clinical teams, ensure trial integrity, and collaborate with regulatory and cross-functional partners to advance product strategy.

The role requires extensive clinical trial experience, deep regulatory knowledge, and strong leadership with excellent English communication. Remote flexibility varies by location and program needs.

Qualifications

• MD/DO or equivalent with relevant therapeutic specialty; residency required; subspecialty fellowship desirable.
• 7+ years of clinical trial experience; 9+ years preferred.
• Ability to run a complex clinical research program independently.
• Proven leadership and ability to lead cross-functional global teams.
• Commitment to training and development of junior staff.
• Ability to interact with internal and external stakeholders to support global strategy.
• Extensive knowledge of clinical trial methodology and regulatory requirements.
• Excellent English verbal and written communication skills.

Responsibilities

• Leads and mentors clinical study teams; ensures study integrity and timelines.
• Oversees design, analysis, interpretation, and reporting of clinical study content and regulatory submissions.
• May chair Clinical Strategy Teams and collaborate with Asset Development Teams.
• Represents clinical development to internal stakeholders and external partners.
• Ensures compliance with GCP, pharmacovigilance standards, and quality procedures.

Skills

Leadership

Cross-functional collaboration

Regulatory knowledge

English communication

Strategic thinking

Education

MD/DO or international equivalent

Job description

AbbVie is seeking a senior medical director to lead multiple clinical development programs, guiding design, analysis, and reporting of pivotal studies. You will mentor clinical teams, ensure trial integrity, and collaborate with regulatory and cross-functional partners to advance product strategy.

The role requires extensive clinical trial experience, deep regulatory knowledge, and strong leadership with excellent English communication. Remote flexibility varies by location and program needs.