Chief Clinical Development Leader

Allergan; North Chicago (IL); On-site; USD 180,000 - 240,000; Full time

Job summary

AbbVie in the United States is seeking an experienced leader to guide clinical development programs across multiple therapeutic areas. You will spearhead cross-functional teams, ensure study integrity, and manage regulatory submissions, while aligning with product strategy.

The role requires deep knowledge of trial methodologies, regulatory standards, and strong English communication to coordinate global teams and stakeholders.

Qualifications

• MD/DO or non-US equivalent with relevant therapeutic specialty; residency preferred; subspecialty fellowship desirable.
• 5+ years (7 years preferred) of clinical trial experience in pharma, academia, or equivalent.
• Ability to run a complex clinical research program independently.
• Proven leadership and ability to lead cross-functional global teams.
• Excellent oral and written English communication skills.
• Extensive knowledge of clinical trial methodology and regulatory/compliance requirements.

Responsibilities

• Leads and directs design and implementation of multiple clinical development programs within the overall product development plan.
• Oversees study teams, ensures enrollment targets and timelines, and reports safety/efficacy data.
• Owns design, analysis, interpretation, and reporting of scientific content for protocols, CSRs, and regulatory submissions.
• May supervise Medical/Scientific Directors and Clinical Scientists on related programs.
• Participates in Clinical Strategy Teams and CST Chair duties, coordinating cross-functional plans.
• Represents clinical development to due diligence and translational strategy efforts as needed.

Skills

Leadership

Cross-functional collaboration

English communication

Problem solving

Clinical trial methodology

Education

MD/DO or non-US equivalent

Job description

AbbVie in the United States is seeking an experienced leader to guide clinical development programs across multiple therapeutic areas. You will spearhead cross-functional teams, ensure study integrity, and manage regulatory submissions, while aligning with product strategy.

The role requires deep knowledge of trial methodologies, regulatory standards, and strong English communication to coordinate global teams and stakeholders.