Clinical Study Project Lead I

Allergan; Irvine (CA); On-site; USD 110,000 - 140,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Long-term incentive programs

Job summary

AbbVie in Irvine, CA is seeking a Study Project Manager I to drive the interface between science and operations for clinical studies across development stages. You will lead cross-functional Clinical Study Teams, ensuring quality, on-time delivery and budget adherence while applying ICH/GCP standards and AbbVie policies.

The role demands strategic thinking, strong communication, and ability to manage external vendors and stakeholders, with a focus on patient-centric study execution and

Qualifications

• Bachelor’s Degree or equivalent degree is required.
• 6 years of pharma-related and/or clinical research experience.
• Preferred exposure in Phase 1-4 studies and/or Medical Device trials.

Responsibilities

• Defines and drives the operational strategies and deliverables for one or more clinical studies.
• Responsible for executing clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies).
• Proactively manages budget, timelines and study issues; brings scientific acumen and global mindset to drive study objectives.
• Leads the cross-functional Clinical Study Team and oversees vendor relationships.
• Coaches and supports cross-functional team members and contributes to Development Operations community.

Skills

Budget management

Cross-functional leadership

Stakeholder management

ICH/GCP knowledge

Education

Bachelor’s Degree or equivalent

Job description

AbbVie in Irvine, CA is seeking a Study Project Manager I to drive the interface between science and operations for clinical studies across development stages. You will lead cross-functional Clinical Study Teams, ensuring quality, on-time delivery and budget adherence while applying ICH/GCP standards and AbbVie policies.

The role demands strategic thinking, strong communication, and ability to manage external vendors and stakeholders, with a focus on patient-centric study execution and