Clinical Study Project Lead I

AbbVie; Irvine (CA); On-site; USD 110,000 - 150,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Job summary

AbbVie in Irvine is seeking a Study Project Manager I to drive the connection between science and operational delivery across development stages. You will lead cross-functional Clinical Study Teams, ensuring quality, on-time delivery within budget while addressing risks.

You will manage study design, budgets, vendor relationships, and stakeholder engagement, while promoting innovation and a patient-centered approach in a global matrix environment.

Qualifications

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

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, 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
• Effectively manages vendors and a diverse set of external stakeholders including site staff, Key Opinion Leaders and patient groups

Skills

Clinical study operations

Budget management

Stakeholder management

Education

Bachelor’s Degree or equivalent

Job description

AbbVie in Irvine is seeking a Study Project Manager I to drive the connection between science and operational delivery across development stages. You will lead cross-functional Clinical Study Teams, ensuring quality, on-time delivery within budget while addressing risks.

You will manage study design, budgets, vendor relationships, and stakeholder engagement, while promoting innovation and a patient-centered approach in a global matrix environment.