Global Study Manager

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Act as the primary point of contact for clients and serve as a liaison among clients, CROs, and Labcorp.

• Provide guidance to ensure smooth delivery of studies.

• Supervise project management for global, high-complexity studies.

• Oversee client deliverables, budgets, risks, and milestones.

• Facilitate communication between clients and extended Labcorp study teams.

• Review statements of work to ensure quality implementation of client requirements.

• Serve as a client ambassador within Labcorp CLS and various business units.

• Document and respond to customer expectations while adhering to regulatory requirements.

• Implement, monitor, and report on performance metrics.

• Engage in continuous process improvement, quality, and productivity initiatives.

• Comprehend the culture and pipeline of assigned clients with both internal and external stakeholders.

• Foster relationships to guarantee that deliverables are timely and budget-compliant.

• Participate in functional meetings and keep processes current.

• Adhere to the LCLS Global Project Management strategy.

• Undertake other responsibilities as assigned.

⛳️ Requirements

• Bachelor’s degree.

• At least 5 years of experience in the pharmaceutical, biotechnology, or CRO industry.

• Minimum of 5 years of experience managing complex global clinical projects, including budget, risk, timeline, and stakeholder management.

• Over 5 years of experience in client-facing roles and stakeholder management.

• Proven ability to drive project execution, influence cross-functional teams, and achieve results in a dynamic, fast-paced environment.

• Capability to lead client communications, manage expectations, influence outcomes, and build long-term trusted partnerships.

• Demonstrated leadership abilities, including influencing without direct authority, aligning cross-functional teams, and eliminating obstacles.

• Proven track record of contributing to broader client, operational, and organizational goals.

• Customer-focused and solution-oriented mindset.

• Demonstrated success in process improvement, change management, or operational excellence initiatives.

• Solid understanding of clinical trials, project management methodologies, and clinical development processes.

• Strong ownership mentality with accountability, independent decision-making, and effective execution of complex projects.

• Proven ability to think strategically, foresee challenges, and create proactive solutions.

• Work schedule from Monday to Friday.

🏝️ Benefits

• Mentoring, training, and personalized development planning.

• Equal opportunity employment.

• Disability accommodations available for applicants.