Senior Global Study Manager, Central Lab Service

🔥 14 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟠 Senior

👔 Manager

🇬🇧 UK Skilled Worker Visa Sponsor

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Logo of Labcorp

Labcorp

10,000+ employees

Founded 1969

💼 Consulting

📦 Logistics

🏥 Healthcare

💰 Post-IPO Debt on 2019-06

Consulting • Logistics • Healthcare

Labcorp is a leading global life sciences company that provides comprehensive clinical laboratory and end-to-end drug development services. The company offers a wide range of diagnostic tests and services for patients, providers, and biopharmaceutical companies. Labcorp specializes in areas such as oncology, women's health, neurology, and genetics, offering both routine and specialized laboratory testing. It supports healthcare systems and organizations with clinical lab testing, health assessments, and employee wellness programs. Labcorp also plays a significant role in the biopharma sector, providing nonclinical research, central laboratory services, and consulting for drug development and commercialization. With their commitment to science and innovation, Labcorp aims to improve health and change lives worldwide.

📋 Description

• Serve as the key client contact and liaison between clients, CROs and Labcorp • Lead interactions among Labcorp study team members to ensure seamless study delivery • Provide project management oversight focused on client deliverables, budget, risk and milestone management • Facilitate communications between clients and the extended Labcorp study team • Review statements of work to ensure quality implementation of client-specific requirements • Manage a portfolio of global, high-complexity studies • Act as a client ambassador within Labcorp Central Lab Services and across Labcorp business units • Document and act on customer expectations in compliance with regulatory requirements • Manage conflicting priorities and make difficult decisions in dynamic environments • Implement, monitor and report performance metrics • Contribute to continuous process improvement, quality and productivity initiatives • Work with internal and external personnel to understand assigned clients' culture and pipeline • Build internal and external relationships to deliver on time and within budget • Participate in functional meetings and keep processes up to date • Comply with the LCLS Global Project Management strategy • Support a culture of continuous improvement, quality and productivity • Support Central Labs projects for Phase I–IV clinical trials and a key leading-pharma client account

🎯 Requirements

• Bachelor degree • 5 or more years of experience in the pharmaceutical, biotechnology, or CRO industry • 5 or more years of experience managing complex global clinical projects, including budget, risk, timeline and stakeholder management • 5 or more years of experience in client-facing and stakeholder management • 2 or more years of Central Labs experience • Proven ability to drive project execution, influence cross-functional teams and deliver results in a dynamic, fast-paced environment • Ability to lead client communications, manage expectations, influence outcomes and build long-term trusted partnerships • Demonstrated leadership skills, including influencing without direct authority, aligning cross-functional teams and removing roadblocks • Proven ability to contribute to broader client, operational and organizational objectives • Customer-focused and solution-oriented approach • Demonstrated success in process improvement, change management or operational excellence initiatives • Excellent understanding of clinical trials, project management methodologies and clinical development processes • Strong ownership, accountability, independent decision-making and complex project execution skills • Proven ability to think strategically, anticipate challenges and develop proactive solutions • Project Management training or certification (PMP, Prince2) preferred • Master degree or University degree preferred

🏖️ Benefits

• Mentoring, training and personalized development planning • Career growth opportunities • Fully remote work arrangement • Monday–Friday work schedule

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