Senior Global Study Manager – Clinical Research, Central Labs Services

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

📋 Description

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

• Provide strategic leadership to ensure effective and timely delivery of studies.

• Oversee project management for complex global studies with high levels of difficulty.

• Manage budgets, identify risks, track milestones, timelines, and ensure client deliverables are met.

• Facilitate effective communication between clients and the broader Labcorp study team.

• Assess and review Statements of Work (SOWs) to ensure high-quality implementation of client requirements.

• Represent clients within Central Labs Services and across various Labcorp business units.

• Document client expectations and ensure compliance with regulatory standards.

• Navigate conflicting priorities and make challenging decisions in fast-paced environments.

• Implement, monitor, and report on performance metrics.

• Engage in continuous improvement initiatives to enhance quality and productivity.

• Familiarize yourself with assigned clients’ culture and project pipeline.

• Cultivate internal and external relationships to ensure project delivery within budget and on time.

• Attend functional meetings and provide insights to keep processes up to date.

• Adhere to the LCLS Global Project Management strategy.

• Perform additional duties as required.

⛳️ Requirements

• High school diploma or equivalent required.

• A minimum of 5 years of experience in the pharmaceutical, biotechnology, or CRO sectors.

• At least 5 years of experience in managing complex global clinical projects, including aspects like budget, risk, timeline, and stakeholder management.

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

• At least 2 years of experience in a Central Labs environment.

• Proven track record of driving project execution, influencing cross-functional teams, and achieving results in dynamic, fast-paced settings.

• Strong ability to lead client communications, manage expectations, influence outcomes, and build trusted partnerships.

• Demonstrated leadership abilities, including the capacity to influence without direct authority, align cross-functional teams, and eliminate obstacles.

• Proven capability to contribute to overarching client, operational, and organizational goals.

• A customer-centric and solution-focused mindset.

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

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

• Strong ownership mentality with accountability and independent decision-making in executing complex projects successfully.

• Ability to think strategically, foresee challenges, and devise proactive solutions.

• Bachelor’s degree in life sciences is preferred.

• Project Management training or certification, such as PMP or Prince2, is preferred.

🏝️ Benefits

• Medical insurance coverage.

• Dental insurance coverage.

• Vision insurance coverage.

• Life insurance provision.

• Short-term disability (STD) coverage.

• Long-term disability (LTD) coverage.

• Participation in a 401(k) plan.

• Paid Time Off (PTO) or Flexible Time Off (FTO) options.

• Tuition reimbursement program.

• Employee Stock Purchase Plan.