Project Coordinator, Clinical Supply

🔥 6 minutes ago

🌽 Illinois – Remote

🌽 Illinois – Remote

💵 $58.7k - $103.5k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

👷‍♀️ Project Manager

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

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AbbVie

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2013

🏥 Healthcare

💼 Consulting

🏭 Manufacturing

Healthcare • Consulting • Manufacturing

AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.

📋 Description

• Manage key Clinical Supply Chain documentation, tasks, and simple packaging activities in a GMP environment • Plan, schedule, coordinate, and execute activities supporting CSPMs • Ensure timely availability of investigational drug supplies and related services to clinical sites and depots • Translate stability and packaging requests into executed packaging designs • Identify, develop, communicate, and track task completion dates, activities, logistics, and milestones • Create protocol-specific manufacturing and packaging work orders with the CSPM • Complete tasks for the Center of Excellence team upon CSPM request • Coordinate with Clinical Drug Supply Chain teams and Germany counterparts to support clinical drug transfers from Lake County

🎯 Requirements

• Bachelor’s Degree required, preferably in physical science, math, engineering or pharmacy • 0–2+ years total experience in the Pharmaceutical Industry • Experience or knowledge of clinical supply chain documentation, tasks, and packaging activities in a GMP environment • Ability to plan, schedule, coordinate, and execute clinical supply chain activities • Ability to create protocol-specific manufacturing and packaging work orders • Ability to identify, develop, communicate, and track task completion dates, activities, logistics, and milestones • Ability to collaborate with Clinical Drug Supply Chain, R43E, Analytical, Quality, and Germany counterparts

🏖️ Benefits

• Paid time off (vacation, holidays, sick) • Medical, dental, and vision insurance • 401(k) • Short-term incentive programs • Remote work eligibility