Clinical Data Risk & Solutions Analyst – Global Monitor

🔥 13 minutes ago

🇮🇳 India – Remote

⏰ Full Time

🟠 Senior

🔴 Lead

🧐 Business Analyst

👻 Ghost score 10%

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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

• Manage an assigned portfolio of clinical studies • Work with internal teams to identify study risks and develop mitigation plans • Identify issues in study data and suggest internal or external corrective and preventive actions • Put customized, study-specific monitoring packages in place based on study needs or client requests • Determine which laboratory samples are at risk of not being resulted on time • Select appropriate monitoring offerings and write clear monitoring instructions for handoff to another team • Monitor and report clinical study laboratory metrics • Extract and analyze information from multiple data sources and present key findings to internal and external stakeholders • Perform risk assessments on low-complexity studies before study start with the Global Study Manager and Study Design Lead • Use analytics and visualizations to identify study issues and proactively address risks • Liaise with developers to ensure monitoring tools meet client specifications • Maintain regular communication with key stakeholders • Support creation and maintenance of Risk Management Plans • Participate in continuous process improvements and functional meetings • Keep processes up to date and comply with internal strategy • Support a culture of continuous improvement, quality, and productivity

🎯 Requirements

• Master’s Degree or PhD in a scientific field • 10 years of related experience in project management or data analysis for the pharmaceutical/healthcare industry; education can substitute for work experience • Advanced level knowledge of Excel • Previous client-facing experience • Strong working proficiency in English • Ability to extract information from multiple data sources and convert raw data into actionable insights • Ability to perform risk assessments and propose monitoring solutions • Ability to use analytics/visualizations to review study laboratory data • Ability to work with developers on monitoring tools • Strong problem-solving and customer service skills • Ability to operate with minimal guidance and own deliverables end-to-end • Ability to communicate ideas effectively and motivate/influence others • Ability to manage conflicting priorities and dynamic timelines • Ability to create and motivate a team around project deliverables

🏖️ Benefits

• Meaningful work contributing to improving health and improving lives • Career growth opportunities • Equal employment opportunity and inclusive workplace • Accessibility accommodations for applicants with disabilities