Senior Global Study Manager – Clinical Research, Central Labs Services

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $60k - $100k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

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Labcorp

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💊 Pharmaceuticals

🧬 Biotechnology

💰 $2G Post-IPO Debt - LabCorp on 2024-09

Healthcare • Pharmaceuticals • Biotechnology

Labcorp is a global leader in laboratory services, diagnostics, and drug development. The company provides testing, data and scientific insights to doctors, hospitals, pharmaceutical companies, researchers and patients, reaching more than 160 million patients annually. Labcorp operates a large global laboratory footprint with roughly 71,000 employees across 100+ countries and invests in advanced technologies (including AI and digital solutions) to accelerate drug development, support precision medicines (such as cell and gene therapies and oncology diagnostics), and inform clinical decision-making.

📋 Description

• Serve as the key client contact and liaison between clients, CROs, and Labcorp • Provide leadership to ensure seamless study delivery • Provide project management oversight for global, high-complexity studies • Manage budgets, risks, milestones, timelines, and client deliverables • Facilitate communication between clients and the extended Labcorp study team • Review Statements of Work (SOWs) for quality implementation of client requirements • Act as a client ambassador within Central Labs 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 • Participate in continuous process improvement, quality, and productivity initiatives • Understand assigned clients’ culture and pipeline • Build internal and external relationships to deliver projects on time and within budget • Participate in functional meetings and provide input to keep processes current • Comply with the LCLS Global Project Management strategy • Perform other duties as assigned

🎯 Requirements

• High school diploma or equivalent • 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 experience working within Central Labs • 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 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 mindset with accountability, independent decision-making, and successful execution of complex projects • Ability to think strategically, anticipate challenges, and develop proactive solutions • Bachelor's degree in life sciences (preferred) • Project Management training or certification, such as PMP or Prince2 (preferred)

🏖️ Benefits

• Medical insurance • Dental insurance • Vision insurance • Life insurance • Short-term disability (STD) • Long-term disability (LTD) • 401(k) plan • Paid Time Off (PTO) or Flexible Time Off (FTO) • Tuition reimbursement • Employee Stock Purchase Plan