Clinical Trails Monitor II (Remote)

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.

Labcorp is seeking a Clinical Trials Monitor II to join our team at Yeshwantpur in Bengaluru, Karnataka

PM: 02:00 PM – 11:00 PM

The Clinical Trials Monitor II , Labcorp Smart Supply develops and manages study-specific strategies to ensure clinical trial kits are available when and where they are needed while minimizing unnecessary inventory and waste. The role uses clinical trial protocols, visit schedules, enrollment expectations, site activity, shipping constraints, and study risks to determine appropriate start-up quantities and ongoing resupply approaches.

As a client-facing operational subject-matter expert, the Global Monitor II works with sponsor study teams and cross-functional Labcorp partners to recommend practical solutions, identify risks or gaps, and make independent, data-informed decisions. The role is expected to question or challenge requests when they could create supply risk, unnecessary waste, or operational issues.

Study Feasibility and Protocol Analysis

Review clinical trial protocols, visit schedules, enrollment assumptions, country requirements, and other study documentation to determine whether and how Labcorp Smart Supply should be used.

Identify study characteristics that may affect kit supply, such as enrollment patterns, visit schedules, treatment groups, specialty testing, country restrictions, site models, and protocol amendments.

Determine whether the service should apply to the full study or only selected kits, sites, countries, regions, or visits; document key assumptions, limitations, risks, and mitigations.

Client Consultation and Operational Leadership

Lead discussions with clients and study teams on supply strategy, start-up quantities, resupply approach, service scope, risks, and performance, translating complex clinical and operational information into clear recommendations.

Use study data, protocol requirements, and operational experience to challenge requests or assumptions that could increase supply risk, kit waste, or process inefficiency, and recommend practical alternatives.

Build alignment across stakeholders by clearly communicating decisions, tradeoffs, responsibilities, and required actions.

Start-Up and Resupply Strategy Design

Develop study-specific start-up kit strategies based on expected enrollment, screening assumptions, site activation plans, visit timing, country lead times, and overall study design.

Design ongoing resupply strategies that define when kits should be replenished, how much should be supplied, and how to account for factors such as patient demand, expiration, shipping lead time, and study risk.

Tailor supply strategies by country, site, patient group, visit, or kit type when needed, and keep start-up and resupply approaches aligned as the study changes.