
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
🟡 Mid-level
👷♀️ Project Manager
🦅 H1B Visa Sponsor
👻 Ghost score 55%
Where this job comes from
Posted on IQVIA's careers page, not through a job board
First seen by Remote Rocketship July 24

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 assigned clinical trial laboratory projects from award through closeout, ensuring protocol requirements are understood and applied • Lead study set-up activities, including protocol and budget review, start-up 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, leading client communications, meetings, and issue triage and escalation • Drive timely, customer-focused problem solving and coordinate cross-functional resources to remove study obstacles • Oversee development of protocol-specific laboratory instructional documents and maintenance of laboratory specifications • Support proposal development, bid defense preparation, and development of 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 with good command of English and clinical research terminology • Ability to work effectively in a fast-paced, high-stress environment with a customer-focused mindset • Ability to establish and maintain effective working relationships with coworkers, managers, and clients
• Integrated benefits programs and resources supporting physical, mental, emotional, financial, and social well-being • Health and welfare benefits • Incentive plans, bonuses, and/or other forms of compensation may be offered
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