Experienced Global Study Manager – Clinical Research, Central Labs Services

🔥 45 minutes ago

🇺🇸 United States – Remote

💵 $60k - $94k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 0%

infoinfo
Apply Now
Find Similar Remote Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Logo of Labcorp

Labcorp

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 key contact for clients and liaison between clients, CROs, and Labcorp • Lead interactions between Labcorp study team members to ensure seamless study delivery • Provide project management oversight for client deliverables, budgets, risks, and milestones • Facilitate communications between clients and the extended Labcorp study team, including Study Design Lead and Regional Study Coordinator • Review statements of work (SOWs) for quality implementation of client-specific requirements • Manage a portfolio of global, high-complexity studies • Act as a client ambassador within Labcorp Central Laboratory 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 timelines and priorities • Implement, monitor, and report performance metrics • Participate in 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 ensure deliverables are on time and within budget • Participate in functional meetings and provide input while keeping processes up to date • Comply with LCLS Global Project Management strategy • Perform other duties as assigned

🎯 Requirements

• High school diploma or equivalent • 5 or more years of experience in pharmaceutical, biotechnology, 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 (internal and external stakeholder) and stakeholder management • Proven ability to drive project execution, influence cross-functional teams and deliver results in a dynamic, fast-paced environment • Ability to lead client communications confidently, manage expectations, influence outcomes, and build long-term trusted partnerships • Demonstrated leadership skills, including the ability to influence without direct authority, align cross-functional teams, and remove roadblocks • Proven ability to think beyond immediate project tasks and contribute to broader client, operational, and organizational objectives • Customer-focused and solution-oriented approach, with a commitment to delivering exceptional client experience • 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 a demonstrated record of accountability, independent decision-making, and successful execution of complex projects • Proven ability to think strategically, anticipate challenges, and develop proactive solutions that support client and business objectives • Bachelor’s degree in life sciences (preferred) • Project Management training or certification (PMP, Prince2) (preferred)

🏖️ Benefits

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

Apply Now

Similar Jobs

🔥 2 hours ago

ICON plc

10,000+ employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence and clinical research organisation. Ensuring protocol compliance, data integrity, patient safety, and high-quality study documentation.

🔥 10 hours ago

Abbott

10,000+ employees

🏥 Healthcare

⚕️ Healthcare Insurance

🧬 Biotechnology

Clinical Biostatistician developing statistical evidence for Abbott’s oncology molecular tests. Supporting study design, regulatory submissions, predictive models, and clinical research.

🔥 11 hours ago

Abbott

10,000+ employees

🏥 Healthcare

⚕️ Healthcare Insurance

🧬 Biotechnology

Clinical Biostatistician developing statistical evidence for Abbott’s oncology molecular tests. Supporting study design, clinical trials, regulatory submissions, and predictive models.

🔥 17 hours ago

Fortrea

10,000+ employees

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Clinical Research Associate monitoring Phase I clinical-trial sites for Fortrea. Ensuring participant safety, regulatory compliance, data integrity, and adverse-event reporting across Florida studies.

🔥 17 hours ago

Labcorp

10,000+ employees

💼 Consulting

📦 Logistics

🏥 Healthcare

Global Study Manager overseeing complex clinical trials for Labcorp’s central laboratory services. Managing client relationships, budgets, risks, milestones, and cross-functional study delivery.