Labcorp is hiring for 5 roles in Bengaluru, Karnataka, covering Clinical Trials Monitor II and Clinical Data Risk & Solutions Analyst (Global Monitor) positions. The roles are based at Yeshwantpur, Bengaluru, are full-time, and follow rotational shifts.
Job Details
| Job Detail | Information |
|---|---|
| Company | Labcorp |
| Location | Yeshwantpur, Bengaluru, Karnataka, India |
| Job Type | Full Time |
| Work Schedule | Rotational Shift |
| AM Shift | 05:30 AM – 02:30 PM |
| PM Shift | 02:00 PM – 11:00 PM |
| Application Deadline | October 15, 2026 |
| Total Roles | 5 |
Positions
Labcorp is hiring for the following 5 positions:
1. Clinical Trials Monitor II – 1 Role
Job Requisition ID: 2635762
The Clinical Trials Monitor II role within Labcorp Smart Supply focuses on developing and managing study-specific strategies to ensure clinical trial kits are available when and where needed while minimizing unnecessary inventory and waste.
2. Clinical Data Risk & Solutions Analyst (Global Monitor) – 4 Roles
Job Requisition IDs:
- 2636014
- 2635658
- 2635659
- 2635660
The Clinical Data Risk & Solutions Analyst (Global Monitor) role involves monitoring clinical study laboratory metrics, identifying study risks, developing mitigation plans, analyzing laboratory data, and implementing customized study-specific monitoring packages.
Clinical Trials Monitor II – Responsibilities
Study Feasibility and Protocol Analysis
- Review clinical trial protocols, visit schedules, enrollment assumptions, country requirements, and study documentation.
- Identify study characteristics affecting kit supply, including enrollment patterns, visit schedules, treatment groups, specialty testing, country restrictions, site models, and protocol amendments.
- Determine whether Smart Supply should apply to the full study or selected kits, sites, countries, regions, or visits.
- Document 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.
- Translate complex clinical and operational information into clear recommendations.
- Challenge requests or assumptions that could increase supply risk, kit waste, or process inefficiency.
- Recommend practical alternatives and build alignment across stakeholders.
Start-Up and Resupply Strategy Design
- Develop study-specific start-up kit strategies based on enrollment, screening assumptions, site activation plans, visit timing, country lead times, and study design.
- Design ongoing resupply strategies considering patient demand, expiration, shipping lead time, and study risk.
- Tailor supply strategies by country, site, patient group, visit, or kit type when required.
- Keep start-up and resupply strategies aligned as studies change.
System Configuration and Quality Control
- Configure and maintain Labcorp Smart Supply services in internal systems.
- Manage study parameters, resupply rules, exclusions, service dates, and quality-control settings.
- Perform quality checks and participate in peer review before activation.
- Review system-generated orders and pending requests.
- Investigate and correct errors and supply risks.
- Maintain supporting instructions and operational records.
Active Study Monitoring and Optimization
- Monitor enrollment, site activity, kit inventory, orders, expirations, system notifications, and key study milestones.
- Analyze trends to identify supply risks, ordering behavior, configuration gaps, site-training needs, process deviations, and opportunities to reduce waste.
- Adjust start-up and resupply strategies as study conditions change.
- Maintain study risk documentation and communicate significant decisions, assumptions, and remaining risks.
Exception and Issue Management
- Investigate system exceptions, failed or unmatched orders, site or kit status changes, data issues, and other conditions affecting automated resupply.
- Coordinate corrective actions, including system updates, order intervention, stakeholder escalation, or client communication.
- Make timely, risk-based decisions while protecting kit availability, data accuracy, and service integrity.
Performance Analysis and Continuous Improvement
- Use dashboards, trackers, and source data to evaluate kit utilization, waste, ordering activity, enrollment, site behavior, and service performance.
- Summarize emerging risks, root causes, and recommended actions.
- Use client and site feedback to improve service design, working practices, training, and supporting tools.
Training and Cross-Functional Coordination
- Provide study-specific training and guidance to clients and relevant 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.
Clinical Trials Monitor II – Eligibility
Candidates should have:
- 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 3 years of relevant experience in clinical trial operations, central laboratory operations, global monitoring, study management, clinical supply, or a related operational role.
Preferred Qualifications
- Experience in clinical trial kit supply.
- Experience in central laboratory services.
- Experience in investigator-site operations.
- Experience with patient recruitment or enrollment workflows.
- Experience with study-specific supply forecasting.
- Knowledge of how therapeutic area, patient pathway, study phase, and site operating model can affect recruitment, visit execution, and kit demand.
- Experience 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.
Clinical Trials Monitor II – Required Skills
- Advanced critical thinking.
- Ability to connect study design, patient flow, site activity, enrollment, logistics, system logic, and operational impact.
- Constructive challenge and influencing skills.
- Strong written and verbal communication.
- Client-facing and facilitation skills.
- Sound judgment and attention to detail.
- Strong quality-control practices.
- Data literacy and proficiency in interpreting dashboards, spreadsheets, trends, exceptions, and operational metrics.
- Strong understanding of clinical trial operations.
- Ability to learn complex systems and apply configurable business rules accurately.
- Strong collaboration, accountability, adaptability, and prioritization across multiple global studies and time zones.
Clinical Data Risk & Solutions Analyst – Responsibilities
The Clinical Data Risk & Solutions Analyst (Global Monitor) will be assigned a portfolio of clinical studies and will work with internal teams to identify study risks, develop mitigation plans, and identify issues in study data.
The role also involves implementing customized, study-specific monitoring packages based on study needs or client requests for additional oversight to ensure laboratory samples are processed correctly.
Key responsibilities include:
- Monitor and report clinical study laboratory metrics.
- Extract information from multiple data sources and convert raw data into meaningful and actionable insights.
- Present key findings to internal and external stakeholders.
- Perform risk assessments on low-complexity studies with the Global Study Manager and Study Design Lead before study start.
- Propose monitoring solutions to mitigate identified risks.
- Use analytics and visualizations to review study laboratory data and identify issues.
- Liaise with developers to ensure monitoring tools meet client specifications.
- Maintain regular communication with key stakeholders.
- Support Risk Management Plan creation and ongoing maintenance.
- Participate in continuous process improvement.
- Work efficiently in an environment with dynamic timelines and priorities.
- Participate in functional meetings and provide input.
- Comply with internal strategy.
- Support quality and productivity initiatives.
Clinical Data Risk & Solutions Analyst – Eligibility
Candidates should have:
- Master’s Degree or PhD in a scientific field.
- 3–5 years of related experience in project management or data analysis for the pharmaceutical or healthcare industry.
- Education can substitute for work experience.
Clinical Data Risk & Solutions Analyst – Required Skills
- Advanced-level knowledge of Excel.
- Previous client-facing experience.
- Data-driven analytical thinking.
- Strong attention to detail and quality standards.
- Strong motivation, flexibility, and creativity.
- Ability to identify risks and opportunities for data improvement.
- Strong problem-solving and customer service skills.
- Comfort with ambiguity and changing priorities across studies and portfolios.
- Ability to operate with minimal guidance and own deliverables end-to-end.
- Ability to communicate ideas and concepts effectively and influence stakeholders.
- Dedication to learning and self-improvement.
- Strong self-organization and ability to manage conflicting priorities.
- Ability to create and motivate a team around project deliverables.
- Strong working proficiency in English.