Clinical Trials Monitor II

🔥 0 minutes ago

🇮🇳 India – Remote

⏰ Full Time

🟠 Senior

🔴 Lead

👻 Ghost score 10%

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Labcorp

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1969

💼 Consulting

📦 Logistics

🏥 Healthcare

💰 Post-IPO Debt on 2019-06

Consulting • Logistics • Healthcare

Labcorp is a leading global life sciences company that provides comprehensive clinical laboratory and end-to-end drug development services. The company offers a wide range of diagnostic tests and services for patients, providers, and biopharmaceutical companies. Labcorp specializes in areas such as oncology, women's health, neurology, and genetics, offering both routine and specialized laboratory testing. It supports healthcare systems and organizations with clinical lab testing, health assessments, and employee wellness programs. Labcorp also plays a significant role in the biopharma sector, providing nonclinical research, central laboratory services, and consulting for drug development and commercialization. With their commitment to science and innovation, Labcorp aims to improve health and change lives worldwide.

📋 Description

• Review clinical trial protocols, visit schedules, enrollment assumptions, country requirements, and study documentation to determine whether and how Labcorp Smart Supply should be used • Identify study characteristics affecting kit supply and determine service scope, assumptions, limitations, risks, and mitigations • Lead client and study-team discussions on supply strategy, start-up quantities, resupply approach, service scope, risks, and performance • Develop study-specific start-up kit strategies and ongoing resupply strategies • Configure and maintain Labcorp Smart Supply services, including study parameters, resupply rules, exclusions, service dates, and quality-control settings • Perform quality checks and peer reviews before activation • Review system-generated orders and pending requests; investigate and correct errors and supply risks • Monitor enrollment, site activity, kit inventory, orders, expirations, notifications, and study milestones • Analyze trends and adjust supply strategies as study conditions change • Investigate exceptions, failed or unmatched orders, status changes, data issues, and automated resupply interruptions • Coordinate corrective actions, escalations, and client communications • Evaluate kit utilization, waste, ordering activity, enrollment, site behavior, and service performance • Provide study-specific training and guidance to clients and study partners • Maintain study documentation, configuration records, trackers, client materials, risk logs, and amendment records • Coordinate responsibilities, timelines, handoffs, and issue resolution across global teams and time zones

🎯 Requirements

• Bachelor's degree in life sciences, clinical research, healthcare, pharmacy, nursing, business, supply chain, or a related field; equivalent relevant experience may be considered in accordance with company policy • Minimum 10 years of relevant experience in clinical trial operations, central laboratory operations, global monitoring, study management, clinical supply, or a related operational role • Experience in clinical trial kit supply, central laboratory services, investigator-site operations, patient recruitment or enrollment workflows, or study-specific supply forecasting • Working knowledge of how therapeutic area, patient pathway, study phase, and site operating model can affect recruitment, visit execution, and kit demand • Experience working with rule-based operational services, workflow tools, or clinical systems • Experience facilitating client meetings, delivering training, completing quality reviews, and managing operational risk or change in a regulated environment • Advanced critical thinking and ability to connect study design, patient flow, site activity, enrollment, logistics, system logic, and operational impact • Constructive challenge and influencing skills • Clear, concise, and confident written and verbal communication, with strong facilitation and client-facing skills • Sound judgment, attention to detail, and disciplined quality-control practices • Data literacy and proficiency in interpreting dashboards, spreadsheets, trends, exceptions, and operational metrics • Strong understanding of clinical trial operations, including study start-up, site activation, screening, enrollment, patient visits, amendments, closeout, site challenges, shipping constraints, and clinical supply risk • Ability to learn complex systems and apply configurable business rules accurately • Strong collaboration, accountability, adaptability, and prioritization across multiple global studies and time zones

🏖️ Benefits

• Equal Opportunity Employer • Accommodation assistance for individuals with disabilities • Inclusive and non-discriminatory workplace