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[Hiring] Clinical Trials Monitor III @Labcorp

Work from home Full-time role Hiring

Role Description Labcorp is seeking a remote Senior Clinical Data Risk & Solutions Analyst (Global Monitor) to join our team! Work Schedule: Monday – Friday, day shift Job Responsibilities

  • Accountable for the monitoring and reporting of clinical study laboratory metrics on a monthly and ad hoc basis.
  • Extract, analyze, and interpret data from multiple sources, transforming raw data into meaningful, actionable insights; present findings to key stakeholders, including the Global Study Manager, Study Design Lead, and external clients.
  • Conduct risk assessments in collaboration with the Global Study Manager and Study Design Lead prior to study initiation; develop and propose monitoring solutions to mitigate identified risks.
  • Utilize analytics and data visualization tools to proactively review study laboratory data, identify trends or issues, and ensure timely risk mitigation.
  • Maintain regular and effective communication with internal stakeholders to ensure alignment and study success.
  • Engage with external clients as needed, including presenting monitoring plans during bid defenses and throughout the study lifecycle.
  • Contribute to organizational growth through participation in continuous improvement initiatives and process optimization within Labcorp.
  • Provide mentorship and guidance to newly hired Global Monitors.
  • Operate effectively in a fast-paced environment with shifting timelines and priorities.
  • Participate in and present at functional meetings (e.g., Labcorp Learning Forums), providing input to enhance and maintain current processes.
  • Ensure compliance with CCLS Global Project Management strategies and standards.
  • Promote and support a culture of continuous improvement, quality, and productivity.
  • Perform additional duties as assigned.

Qualifications

  • Bachelor degree in science
  • 5 or more years’ experience monitoring clinical trials data and/or reporting metrics

Requirements

  • Master’s degree in science (preferred)
  • 3 or more years of experience in Excel (preferred)
  • 1 or more years of experience in client management (preferred)
  • Advanced proficiency in Excel (including working knowledge of Power Query)
  • Experience creating complex study addendums independently with high quality and minimal revisions
  • Ability to perform study monitoring and deliver insightful, value‑added analysis in clear, client‑friendly communications
  • Strong capability to independently conduct risk assessments and provide actionable recommendations
  • Accurate and consistent data entry and workload tracking (e.g., Workfront)
  • Proven mentorship skills, with the ability to develop new hires to work with minimal supervision
  • Analytical, data-driven mindset with a natural curiosity
  • Strong problem-solving and critical thinking skills
  • High attention to detail and commitment to quality standards
  • Ability to manage multiple priorities and work effectively in a fast-paced environment
  • Strong communication skills, with the ability to clearly convey ideas and influence outcomes
  • Self-motivated with a commitment to continuous learning and improvement
  • Customer-focused with strong stakeholder management skills
  • Proficiency in data visualization and analytics tools (e.g., Spotfire, Tableau, R)

Benefits

  • Comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan for employees regularly scheduled to work 20 or more hours per week.
  • Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan.

Application Window June 25, 2026 – June 30, 2026 Pay Range $90,000 - $110,000

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