Clinical Study Project Lead — Cross-Functional Ops

BioSpace

North Chicago (IL)

On-site

USD 110,000 - 140,000

Full time

8 days ago

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Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k) plan

Job summary

AbbVie is seeking a Study Project Manager I to bridge science and operational delivery across development stages. You will lead cross-functional Clinical Study Teams, drive study planning, and ensure execution with quality, on-time delivery, within budget, and aligned with company objectives.

The role requires 6+ years in pharma/clinical research and a Bachelor's degree or equivalent. You will engage in budget oversight, vendor management, and risk mitigation while promoting a growth mindset

Qualifications

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

Responsibilities

Defines and drives operational strategies and deliverables for one or more clinical studies.
Ensures studies are conducted in compliance with quality standards (ICH/GCP, Global Regulations, AbbVie policies).
Manages budgets, timelines, and study issues; applies scientific acumen and global mindset to achieve objectives.
Leads cross-functional Clinical Study Teams through planning to execution.
Oversees vendor selection, scope, and management; interacts with site staff and key opinion leaders.
Identifies risks and implements actions to accelerate study-related issues and opportunities for efficiency.
Mentors Study Management Associates and fosters a collaborative, innovative environment.