Clinical Data Risk & Solutions Analyst (Global Monitor)

Overview

Clinical Data Risk & Solutions Analyst (Global Monitor) role at Labcorp, responsible for monitoring clinical study laboratory data and managing study risks across an assigned portfolio of clinical studies.

What you'll do

• Identify study risks with internal teams when a new study starts and develop mitigation plans.
• Look for issues in study data and suggest internal and/or external actions to rectify and prevent them and maintain study health.
• Put in place customized, study-specific monitoring packages based on study needs or client requests for additional oversight.
• Understand which laboratory samples are at risk of not being resulted on time, choose the best-suited monitoring offering, and write clear monitoring instructions for handoff.
• Be accountable for monitoring and reporting clinical study laboratory metrics.
• Extract information from multiple data sources, convert raw data into actionable insights, and present key findings to internal and external stakeholders.
• Perform risk assessments on low complexity studies with the Global Study Manager and Study Design Lead prior to study start and propose monitoring solutions.
• Use analytics and visualizations to review study laboratory data to identify issues and proactively address risks.
• Liaise with Developers to ensure monitoring tools are developed to client specifications.
• Ensure regular communication with key stakeholders.
• Support Risk Management Plan creation and ongoing maintenance through monitoring and analysis.
• Participate actively in Labcorp development through continuous process improvements.
• Act efficiently in an environment with dynamic timelines and priorities.
• Participate in functional meetings, provide input, and keep processes up to date.
• Comply with internal strategy and CCLS Global Project Management strategy.
• Support a culture of continuous improvement, quality and productivity.

What you'll need

• Master's Degree or PhD in a scientific field.
• 10 years of related experience (education can substitute for work experience) in project management or data analysis for the pharmaceutical/healthcare industry.
• Demonstrated advanced level knowledge of Excel.
• Previous client-facing experience.
• Curious, data-driven analytical thinker.
• High quality standards and attention to detail.
• Strong motivation, flexibility and creativity.
• Big-picture thinker who suggests process changes, identifies risks and data improvement opportunities.
• Strong problem-solving and customer service skills.
• Comfort with ambiguity and fast switching across studies/portfolios as priorities change.
• Able to operate with minimal guidance while owning deliverables end-to-end.
• Proven ability to communicate ideas and to motivate and influence others to accomplish challenging shared goals.
• Dedication to learning and self-improvement.
• Robust self-organization; at ease with managing conflicting priorities.
• Ability to create and motivate a team around project deliverables.
• Strong working proficiency in English.

Details

• Work mode: Remote, based at Bangalore (Yeshwantpur), Karnataka, India.
• Work schedule: 02:00 PM – 11:00 PM.