Clinical Study Project Manager I — Lead Cross-Functional Studies

AbbVie Inc.; North Chicago (IL); On-site; USD 110,000 - 209,000; Full time

Job summary

AbbVie in the United States seeks a Study Project Manager I to bridge science and operations, driving planning and execution of clinical studies across development stages. You will lead cross-functional teams to deliver studies on time, within budget, and to quality standards.

This role emphasizes risk management, stakeholder collaboration, and continuous process improvement, with accountability for study design, budgets, vendor oversight, and execution by the Study Management Associates.

Qualifications

• Bachelor’s Degree or equivalent required.
• 6 years pharma-related and/or clinical research experience required.
• Preferred exposure in Phase 1-4 and/or Medical Device Trial Experience.

Responsibilities

• Defines and drives operational strategies and deliverables for one or more clinical studies.
• Responsible for executing studies in compliance with ICH/GCP and AbbVie policies.
• Proactively manages budget, timelines and study issues; leads cross-functional Clinical Study Team.

Skills

Clinical study operations

Stakeholder management

Budget management

Education

Bachelor’s Degree or equivalent

Job description

AbbVie in the United States seeks a Study Project Manager I to bridge science and operations, driving planning and execution of clinical studies across development stages. You will lead cross-functional teams to deliver studies on time, within budget, and to quality standards.

This role emphasizes risk management, stakeholder collaboration, and continuous process improvement, with accountability for study design, budgets, vendor oversight, and execution by the Study Management Associates.