Clinical Data Risk & Solutions Analyst – Global Monitor

🔥 53 minutes ago

🇮🇳 India – Remote

⏰ Full Time

🟠 Senior

🔴 Lead

🧐 Business Analyst

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Logo of Labcorp

Labcorp

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 at study start to identify study risks and develop mitigation plans • Identify issues in study data and suggest internal and/or external actions to rectify and prevent them • Maintain study health • Implement customized, study-specific monitoring packages based on study needs or client requests for additional oversight • Determine which laboratory samples are at risk of not being resulted on time • Select the monitoring offerings best suited to study needs • Write clear monitoring instructions for handoff to another team • Monitor and report clinical study laboratory metrics • Extract information from multiple data sources, convert raw data into meaningful and 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 before study start • Propose monitoring solutions to mitigate identified risks • Use analytics and visualizations to review study laboratory data, identify issues, and proactively address risks • Liaise with Developers to ensure monitoring tools meet client specifications • Communicate regularly with key stakeholders • Support creation and ongoing maintenance of Risk Management Plans through monitoring and analysis • Participate in continuous process improvements and functional meetings • Keep processes up to date and comply with internal strategy • Operate effectively with dynamic timelines and changing priorities • 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 • Curious, data-driven analytical thinking • High quality standards and attention to detail • Strong motivation, flexibility and creativity • Big-picture thinking and ability to suggest process changes, identify risks and data-improvement opportunities • Strong problem-solving and customer service skills • Comfort with ambiguity and rapidly switching across studies/portfolios as priorities change • Ability to operate with minimal guidance and own deliverables end-to-end • Ability to communicate ideas/concepts effectively and motivate/influence others toward shared goals and objectives • 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

🏖️ Benefits

• Equal Opportunity Employer • Consideration for qualified applicants without regard to protected characteristics • Disability accommodations for online job application tools

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