Clinical Data Risk & Solutions Analyst (Global Monitor)

• Accountable for the monitoring and reporting of clinical study laboratory metrics.
• Ability to extract information from multiple data sources, converting the raw data into meaningful and actionable insights, and presenting key findings to all stakeholders (internal and external).
• Performing risk assessments on low complexity studies in coordination with the Global Study Manager and the Study Design Lead prior to study start and proposing monitoring solutions to mitigate the identified risks.
• Utilizing analytics/visualizations to review study laboratory data for your assigned studies to identify issues and to ensure risks are proactively addressed.
• Liaise with Developers to ensure development of monitoring tools are completed to the client's specifications
• Ensure regular communication with your key stakeholders.
• Support Risk Management Plan creation and ongoing maintenance through monitoring and analysis
• Participate actively to Labcorp development through continuous process improvements.
• Be able to act efficiently in an environment with dynamic timelines and priorities.
• Participate in functional meetings and provide input, keeping processes up to date.
• Comply with internal strategy.
• Support a culture of continuous improvement, quality and productivity., Labcorp manages one of the largest networks of clinical laboratories in the world.

In the Clinical Data Risk & Solutions Analyst (Global Monitor) role, you will be assigned a portfolio of clinical studies. When a new study starts, the Global Monitor works with the internal teams to identify study risks and develop mitigation plans. Global Monitors also look for issues in the study data and suggest actions internally and/or externally to rectify and prevent those issues and maintain study health.

Additionally, you will be responsible for putting in place customized, study specific monitoring packages for studies based on study needs or in which clients are requesting additional oversight by Labcorp to ensure all their samples will be processed correctly. To do this, you will need to understand which laboratory samples are at risk for not being resulted on time, to choose which of our monitoring offerings is best suited for the study needs, and then to write clear monitoring instructions that will be handed off to another part of the team. Overall, the Global Monitor must be in compliance with the CCLS Global Project Management strategy and deliver outstanding performance and customer satisfaction.

• University degree in science
• 3 or more years of experience in clinical project management or clinical data analysis
• 1 or more years of experience in the life science, healthcare or pharmaceutical industry, * PhD degree in science
• 3 or more years of experience in Excel
• 1 or more years of experience in client management

Additional Job Standards:

• Fluency in English
• Curious, data driven analytical thinker
• High quality standards, attention to detail
• Strong motivation, flexibility and creativity
• Big picture thinker who suggests changes to process, identifies risks and potential opportunities for data improvement
• 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 effectively communicate ideas/concepts and to motivate/influence others to accomplish challenging shared goals and objectives.
• Dedication for learning and self-improvement
• Robust self-organization; at-ease with managing conflicting priorities
• Ability to create and motivate a team around project deliverables