Clinical Study Project Lead I

AbbVie; Irvine (CA); On-site; USD 110,000 - 209,000; Full time

Job summary

AbbVie is seeking a Study Project Manager I to bridge science and operations, ensuring excellent delivery of clinical studies across development stages. You will lead cross-functional teams and manage study planning, budgets and timelines in a global matrix environment.

The role emphasizes scientific acumen, stakeholder management, and a proactive risk-driven approach to optimize study execution and patient-centric outcomes.

Qualifications

• Bachelor’s degree or equivalent required.
• 6+ years pharma-related and/or clinical research experience.
• 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.
• Responsible for executing clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, AbbVie policies and procedures).
• Proactively manages budget, timelines and study issues; brings scientific acumen, technical expertise and global mindset to drive achievement of study objectives.
• Leader of the cross functional Clinical Study Team.
• Leads clinical operations planning through to execution via cross functional matrix environment and influences cross functional stakeholders to drive milestone achievement.

Skills

Pharma/clinical research

Budget management

Education

Bachelor’s Degree

Job description

AbbVie is seeking a Study Project Manager I to bridge science and operations, ensuring excellent delivery of clinical studies across development stages. You will lead cross-functional teams and manage study planning, budgets and timelines in a global matrix environment.

The role emphasizes scientific acumen, stakeholder management, and a proactive risk-driven approach to optimize study execution and patient-centric outcomes.