Project Manager, Study I

🔥 20 hours ago

🌽 Illinois – Remote

🌽 Illinois – Remote

💵 $109.5k - $208.5k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

👷‍♀️ Project Manager

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👻 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

• Define and drive operational strategies and deliverables for one or more clinical studies • Execute clinical studies in compliance with quality standards, ICH/GCP, global regulations, and company policies • Manage study budgets, timelines, issues, risks, and opportunities • Lead one or more cross-functional Clinical Study Teams • Lead clinical operations planning through execution in a cross-functional matrix environment • Manage vendors and external stakeholders, including site staff, Key Opinion Leaders, and patient groups • Coach, support, delegate to, and empower cross-functional team members • Contribute to operational efficiencies and innovative ideas • Develop clinical study designs and associated systems, tools, and documents • Create and oversee study budgets • Select, scope, manage, and oversee external vendors • Make operational decisions regarding study execution • Create an inclusive and innovative environment for staff and studies/programs • Provide leadership to Study Management Associates and support activities to deliver study milestones

🎯 Requirements

• Bachelor's Degree or equivalent degree is required • 6 years of demonstrated pharma-related and/or clinical research related experience or equivalent required • Preferred exposure in study initiation through study completion in Phase 1-4 • Preferred exposure to Medical Device Trial Experience • Experience with clinical study operations management • Knowledge of ICH/GCP, Global Regulations, and company policies and procedures • Vendor and external stakeholder management experience • Excellent communication and problem-solving skills • Ability to lead cross-functional teams in a matrix environment

🏖️ Benefits

• Paid time off, including vacation, holidays, and sick leave • Medical, dental, and vision insurance • 401(k) • Eligibility to participate in long-term incentive programs