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Clinical Trial Data Analyst (Global Monitor)
☞ PharmiWeb.jobs: Global Life Science Jobs
View: 138
Update day: 08-04-2024
Category: IT - Software
Industry: Staffing Recruiting
Position: Mid-Senior level
Job type: Full-time
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Job content
If you are looking for a company where you can personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view, consider working at Labcorp as a Clinical Trial Data Analyst (Global Monitor).Labcorp manages one of the largest networks of clinical laboratories in the world.In the Clinical Trial Data Analyst (Global Monitor) role, you will be assigned a portfolio of clinical studies and you will be responsible for ensuring that each month these studies laboratory data is on track by consulting an internal dashboard. Specifically, that the laboratory specimens are collected per protocol and that they are being processed and resulted as expected. If they are not, your role will be to investigate why that is not happening and share those insights with the study Project Managers as to how to rectify and prevent those issues.Additionally, you will be responsible for putting in place customized, study specific monitoring packages of low to moderate complexity for studies 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.In more details, you will be...- Accountable for the monitoring and reporting of clinical study laboratory metrics on both a monthly and/or ad hoc basis.
- Extracting information from multiple data sources, converting the raw data into meaningful and actionable insights, and presenting key findings to your stakeholders (the Global Study Manager (aka the study Project Manager) and the Study Design Lead (aka the study Technical Writer).
- Utilizing analytics/visualizations to review study laboratory data for your assigned studies to identify issues and to ensure risks are proactively addressed.
- Ensuring regular communication with your key internal stakeholders.
- Participating actively to LabCorp development through continuous process improvements.
- Acting efficiently in an environment with dynamic timelines and priorities.
- Participating in functional meetings (e.g. LabCorp Learning Forums) and provide input, keeping processes up to date.
- Complying with Central Laboratory Global Project Management strategy.
- Supporting a culture of continuous improvement, quality and productivity.
- Other duties as assigned.
- University Bachelor Degree; in scientific field is a strong plus.
- 3-5 years of related experience
- Curious, data driven analytical thinker
- Strong problem-solving skills
- Able to operate with minimal guidance while owning deliverables end-to-end
- Proven ability to effectively communicate ideas/concepts and to motivate others to accomplish challenging shared goals and objectives.
- Dedication for learning and self-improvement
- Robust self-organization; at-ease with managing conflicting priorities
- Strong customer service skills
- Working proficiency in English
- Demonstrated advanced level knowledge in Excel
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Deadline: 23-05-2024
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