Labcorp
Labcorp
Labcorp combines laboratory testing, diagnostics, drug development, and scientific data to support healthcare providers, hospitals, pharmaceutical companies, researchers, and patients. Its global operations serve more than 160 million patients each year, with teams working across a broad laboratory network and more than 100 countries. The company applies advanced technologies, including artificial intelligence and digital tools, to accelerate clinical research, enable precision medicine initiatives such as cell and gene therapies and oncology diagnostics, and help inform medical decisions. Labcorp’s careers span healthcare, pharmaceuticals, biotechnology, laboratory science, technology, and drug development.

Senior Global Study Manager, Clinical Research - Labcorp Remote

Lead complex global clinical studies remotely for Labcorp’s Central Labs Services team. Oversee client delivery, budgets, risks, milestones, regulatory expectations, and cross-functional collaboration.

Description

  • Serve as the primary liaison among clients, CROs, and Labcorp.
  • Lead study teams to support consistent, effective delivery.
  • Oversee project management for complex global clinical studies.
  • Control study budgets, risks, milestones, timelines, and client deliverables.
  • Coordinate communication between clients and the broader Labcorp study team.
  • Review Statements of Work to confirm accurate implementation of client requirements.
  • Represent client interests across Central Labs Services and Labcorp business units.
  • Capture and address customer expectations while meeting regulatory obligations.
  • Balance competing priorities and make sound decisions in changing environments.
  • Establish, track, and communicate performance metrics.
  • Support continuous improvement, quality, and productivity programs.
  • Develop an understanding of assigned clients’ cultures and pipelines.
  • Strengthen internal and external partnerships to deliver projects on schedule and within budget.
  • Contribute to functional meetings and help keep processes up to date.
  • Follow the LCLS Global Project Management strategy.
  • Complete additional duties as assigned.

Requirements

  • High school diploma or equivalent qualification.
  • At least five years of experience in the pharmaceutical, biotechnology, or CRO sector.
  • At least five years managing complex global clinical projects, including budgets, risks, timelines, and stakeholders.
  • At least five years of client-facing and stakeholder management experience.
  • At least two years of experience working in Central Labs.
  • Ability to drive project execution, influence cross-functional teams, and achieve results in a fast-paced environment.
  • Ability to lead client communications, manage expectations, influence decisions, and build trusted partnerships.
  • Leadership ability, including influencing without direct authority, aligning cross-functional teams, and clearing obstacles.
  • Ability to support broader client, operational, and organizational goals.
  • Customer-focused, practical approach to solving problems.
  • Track record of contributing to process improvement, change management, or operational excellence initiatives.
  • Strong knowledge of clinical trials, project management methods, and clinical development processes.
  • Accountable ownership, independent judgment, and a record of successfully delivering complex projects.
  • Strategic thinking with the ability to anticipate issues and create proactive solutions.
  • Bachelor’s degree in life sciences preferred.
  • Project management training or certification, such as PMP or PRINCE2, preferred.

Benefits

  • Medical insurance coverage.
  • Dental insurance coverage.
  • Vision insurance coverage.
  • Life insurance coverage.
  • Short-term disability coverage.
  • Long-term disability coverage.
  • 401(k) retirement plan.
  • Paid Time Off or Flexible Time Off.
  • Tuition reimbursement.
  • Employee Stock Purchase Plan.

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