Clinical Study Project Manager I

AbbVie; New Jersey; On-site; USD 120,000 - 160,000; Full time

Job summary

AbbVie is seeking a Study Project Manager I to drive the intersection of science and operational delivery across clinical studies. The role ensures quality, on-time execution, within budget, and alignment with company objectives in a cross-functional matrix environment.

The position requires a Bachelor’s degree and at least six years in pharma-related or clinical research roles, with a track record leading diverse teams and managing stakeholders to mitigate risk and deliver milestones.

Qualifications

• Bachelor’s degree required; equivalent acceptable.
• 6+ years of pharma-related or clinical research experience.
• Experience leading cross-functional clinical study teams preferred.

Responsibilities

• Defines operational strategies and deliverables for clinical studies.
• Manages studies in compliance with ICH/GCP and AbbVie policies.
• Oversees budgets, timelines, and study issues; coordinates with vendors and sites.
• Leads cross-functional Clinical Study Team to achieve milestones.
• Mentors Study Management Associates and supports study execution.

Skills

Clinical research

Pharma experience

Cross-functional leadership

Education

Bachelor’s degree

Job description

AbbVie is seeking a Study Project Manager I to drive the intersection of science and operational delivery across clinical studies. The role ensures quality, on-time execution, within budget, and alignment with company objectives in a cross-functional matrix environment.

The position requires a Bachelor’s degree and at least six years in pharma-related or clinical research roles, with a track record leading diverse teams and managing stakeholders to mitigate risk and deliver milestones.