[Hiring] Clinical Trials Monitor II @Labcorp

Role Description

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

Work Schedule: 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
• Make independent, data-informed decisions
• Question or challenge requests that could create supply risk, unnecessary waste, or operational issues

Qualifications

• 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.

Requirements

• 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.

Benefits

• Advanced critical thinking and the ability to connect study design, patient flow, site activity, enrollment, logistics, system logic, and operational impact.
• Constructive challenge and influencing skills, including the ability to push back professionally, explain evidence and trade-offs, and propose workable alternatives.
• Clear, concise, and confident written and verbal communication, with strong facilitation and client-facing skills and the ability to simplify complex information for different audiences.
• 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.

Company Description

Labcorp is a global leader in laboratory services, providing insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies, and health systems make confident decisions and improve outcomes.

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind.