Clinical Trials Monitor III

Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve health outcomes for people. With our global scale and deep expertise, you'll do meaningful work, grow your career and make a real impact. Together, we're improving health and improving lives. 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. **Minimum Qualifications** * Bachelor degree in science * 5 or more years’ experience monitoring clinical trials data and/or reporting metrics **Preferred Qualifications** * Master’s degree in science * 3 or more years of experience in Excel * 1 or more years of experience in client management **Additional Job Standards** * 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) * Prove