Clinical Trials Monitor II

🕒 Yesterday

🇮🇳 India – Remote

⏰ Full Time

🟠 Senior

🔴 Lead

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Labcorp

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💊 Pharmaceuticals

🧬 Biotechnology

💰 $2G Post-IPO Debt - LabCorp on 2024-09

Healthcare • Pharmaceuticals • Biotechnology

Labcorp is a global leader in laboratory services, diagnostics, and drug development. The company provides testing, data and scientific insights to doctors, hospitals, pharmaceutical companies, researchers and patients, reaching more than 160 million patients annually. Labcorp operates a large global laboratory footprint with roughly 71,000 employees across 100+ countries and invests in advanced technologies (including AI and digital solutions) to accelerate drug development, support precision medicines (such as cell and gene therapies and oncology diagnostics), and inform clinical decision-making.

📋 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 • Challenge requests or assumptions that could increase supply risk, kit waste, or process inefficiency, and recommend alternatives • Develop study-specific start-up kit strategies and ongoing resupply strategies • Tailor supply strategies by country, site, patient group, visit, or kit type • Configure and maintain 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 correct errors or supply risks • Monitor enrollment, site activity, kit inventory, orders, expirations, notifications, and study milestones • Analyze trends, identify supply risks and process gaps, and adjust strategies as study conditions change • Investigate exceptions, failed or unmatched orders, status changes, data issues, and other automated-resupply interruptions • Coordinate corrective actions, escalations, and client communications • Evaluate kit utilization, waste, ordering activity, enrollment, site behavior, and service performance using dashboards, trackers, and source data • Provide study-specific training and guidance to clients and internal and external 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