Clinical Study Project Lead

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

Benefits offered by this job

Medical, dental, and vision insurance

401(k) plan

Paid time off

Job summary

AbbVie is looking for a Study Project Manager II in Irvine, California. The successful candidate will lead the operational strategies for clinical research studies, ensuring quality and timely delivery aligned with company objectives.

In this role, you will leverage your extensive experience in clinical study management, expertise in drug/device studies, and exemplary leadership skills. AbbVie offers a comprehensive benefits package along with competitive compensation.

Qualifications

• 8 years of demonstrated clinical research study management required.
• Experience with cross-functional teams essential.
• Well-versed in ICH/GCP regulations and AbbVie SOPs.

Responsibilities

• Lead clinical operational strategies ensuring timely execution and quality.
• Oversight on vendor collaboration including contract review.
• Identify risks and provide solutions to mitigate them.

Skills

Leadership

Strategic Thinking

Risk Management

Operational Excellence

Education

Bachelor’s Degree or equivalent

Tools

EDC

IRT

CTMS

eTMF

Job description

AbbVie is looking for a Study Project Manager II in Irvine, California. The successful candidate will lead the operational strategies for clinical research studies, ensuring quality and timely delivery aligned with company objectives.

In this role, you will leverage your extensive experience in clinical study management, expertise in drug/device studies, and exemplary leadership skills. AbbVie offers a comprehensive benefits package along with competitive compensation.