Study Project Manager I — Clinical Operations Lead

AbbVie; Florham Park (NJ); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Job summary

AbbVie is seeking a Study Project Manager I to bridge science and operations, ensuring quality, efficiency, and on-time delivery of clinical studies across development stages.

Leverage scientific acumen, stakeholder management, and cross-functional leadership to lead study teams, manage budgets, timelines, and risks in a matrix environment. This role anchors operational excellence within AbbVie’s clinical operations.

Qualifications

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

Responsibilities

• Defines and drives operational strategies and deliverables for one or more clinical studies.
• Executes clinical studies in compliance with ICH/GCP, global regulations and AbbVie policies.
• Manages budget, timelines and study issues; fosters scientific acumen and global mindset.
• Leads the cross-functional Clinical Study Team in planning and execution.
• Oversees vendor selection, scope development and management of external vendors.

Skills

Project management

Clinical studies

Budget management

Vendor management

Regulatory compliance

Education

Bachelor’s Degree

Job description

AbbVie is seeking a Study Project Manager I to bridge science and operations, ensuring quality, efficiency, and on-time delivery of clinical studies across development stages.

Leverage scientific acumen, stakeholder management, and cross-functional leadership to lead study teams, manage budgets, timelines, and risks in a matrix environment. This role anchors operational excellence within AbbVie’s clinical operations.