
10,000+ employees
💼 Consulting
🏭 Manufacturing
📣 Marketing
💰 $1G Post-IPO Debt on 2023-05
Consulting • Manufacturing • Marketing
IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.
🕒 July 24
🏄 California, Washington – Remote
💵 $64.2k - $173k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
👷♀️ Project Manager
🚫👨🎓 No degree required
🦅 H1B Visa Sponsor
👻 Ghost score 30%
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10,000+ employees
💼 Consulting
🏭 Manufacturing
📣 Marketing
💰 $1G Post-IPO Debt on 2023-05
Consulting • Manufacturing • Marketing
IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.
• Manage all laboratory aspects of assigned clinical trial projects from award through closeout • Ensure protocol requirements are understood and applied • Lead study setup, including protocol and budget review, startup meetings, and implementation of project and risk management plans • Monitor timelines, deliverables, metrics, and budgets, including trend analysis, scope changes, and change orders • Serve as the single point of contact for sponsors • Lead client communications, meetings, issue triage, and escalation • Drive timely, customer-focused problem solving and coordinate cross-functional resources • Oversee development of protocol-specific laboratory instructional documents and maintenance of laboratory specifications • Support proposal development, bid defense preparation, and sponsor- or program-specific standards and procedures • Capture lessons learned and support continuous improvement across projects and programs
• Bachelor's Degree in Life Sciences and/or related field preferred • 3+ years of experience in a regulated laboratory environment • 2+ years of experience managing projects, such as study setup, method validation or transfer, or client programs • Computer proficiency with Microsoft Office (Word, Excel, PowerPoint) and comparable company systems in a project delivery environment • Strong interpersonal and client management skills • Experience with Lab Trial Management Systems (LTMS) • Strong organizational skills, accuracy, and attention to detail while managing multiple priorities and deadlines • Strong written and verbal communication skills • Good command of English and clinical research terminology • Ability to work effectively in a fast-paced, high-stress environment • Ability to establish and maintain effective working relationships with coworkers, managers, and clients
• Health and welfare benefits • Resources supporting physical, mental, emotional, financial, and social well-being • Benefits for employees and their families • Potential incentive plans, bonuses, and/or other forms of compensation
Apply Now🕒 July 24
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