
Senior Global Study Manager, Central Lab Service
Posted 1 day ago

Posted 1 day ago
This is a fully remote position, open to applicants in United Kingdom.
• Act as the primary client contact and intermediary among clients, CROs, and Labcorp.
• Oversee interactions among Labcorp study team members to guarantee smooth delivery of studies.
• Provide project management oversight with an emphasis on client deliverables, budget, risk, and milestone management.
• Facilitate communication between clients and the broader Labcorp study team.
• Review statements of work to ensure high-quality execution of client-specific requirements.
• Manage a portfolio of global, highly complex studies.
• Serve as a client ambassador within Labcorp Central Lab Services and throughout Labcorp business units.
• Document and respond to customer expectations in accordance with regulatory standards.
• Navigate conflicting priorities and make challenging decisions in dynamic settings.
• Implement, monitor, and report on performance metrics.
• Contribute to ongoing process enhancements, quality, and productivity initiatives.
• Collaborate with internal and external personnel to grasp the culture and pipeline of assigned clients.
• Cultivate internal and external relationships to ensure timely and budget-compliant delivery.
• Attend functional meetings and keep processes current.
• Adhere to the LCLS Global Project Management strategy.
• Foster a culture of continuous improvement, quality, and productivity.
• Support Central Labs projects for Phase I–IV clinical trials and a major leading-pharma client account.
• Bachelor's degree.
• A minimum of 5 years of experience in the pharmaceutical, biotechnology, or CRO sector.
• At least 5 years of experience managing complex global clinical projects, including budget, risk, timeline, and stakeholder management.
• More than 5 years of experience in client-facing and stakeholder management roles.
• A minimum of 2 years of experience in Central Labs.
• Demonstrated ability to drive project execution, influence cross-functional teams, and achieve results in a fast-paced environment.
• Capability to lead client communications, manage expectations, influence outcomes, and establish long-term trusted partnerships.
• Proven leadership skills, including influencing without direct authority, aligning cross-functional teams, and eliminating roadblocks.
• Established ability to contribute to broader client, operational, and organizational goals.
• Customer-oriented and solution-focused mindset.
• Proven track record in process improvement, change management, or operational excellence initiatives.
• Strong understanding of clinical trials, project management methodologies, and clinical development processes.
• Excellent skills in ownership, accountability, independent decision-making, and complex project execution.
• Established ability to think strategically, foresee challenges, and devise proactive solutions.
• Project Management training or certification (PMP, Prince2) is preferred.
• Master's degree or equivalent university degree is preferred.
• Mentoring, training, and personalized development planning.
• Opportunities for career advancement.
• Fully remote work arrangement.
• Monday to Friday work schedule.
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