Clinical Trial Data Analyst

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).

This is a fully remote position.

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.

Your role as a Clinical Trial Data Analyst

In this role, you will create and maintain the Global Monitoring plan for the assigned studies, coordinate the work of Client Coordinator Specialists, Global Monitoring Center and Regional Study Coordinators and ensure regular communication with the Global Study Managers or Global Study Leads who are accountable for the entire protocol.

 In more details, you will…
• Leverage therapeutic area, client and study type knowledge to create and maintain a study specific monitoring and data lock plan
• Liaise with internal teams to ensure monitoring needs for a study can be met with quality
• Provide data focused impact assessments as needed

• Utilizing analytics/visualizations to review study laboratory data for your assigned studies to identify issues and to ensure risks are proactively addressed.

• 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).

• Accountable for the monitoring and reporting of clinical study laboratory metrics on both a monthly and/or ad hoc basis.
• Triage of new work requests
• Liaise with Developers to ensure development of monitoring tools are completed to the client’s specifications
• Delegate/generate reports related to monitoring activities
• Review/analyze data within monitoring scope
• Suggest actions/changes to the Global Study Manager (Project management team) based on data analysis

• Ensure regular communication with your key internal stakeholders
• Escalate issues, highlight trends and liaise closely with Global Study Manager or Global Study Lead throughout life of the study to ensure monitoring is appropriate
• Support Risk Management Plan creation and ongoing maintenance through monitoring, analysis
• Participate in functional meetings (e.g. CLFs) and provide input, keeping processes up to date
• Comply with the Central Laboratory Global Project Management strategy
• Support a culture of continuous improvement, quality and productivity

Thrive personally and professionally at Labcorp Drug Development

Working at Labcorp Drug Development, you’ll continue to grow in our learning-based culture so you’ll know how to expertly respond and adapt as the industry continues to evolve. Here, you’ll put your education to work as you play a meaningful role in advancing healthcare and making a difference in people’s life.

In addition, Labcorp Drug Development offers great benefits, global experience and the opportunity to work independently within a team-oriented environment.

What we’re looking for
Clinical Trial Data Analysts (Global Monitors) are the most successful at Labcorp with:
• University Degree required; Masters or PhD in scientific field preferred
• 3-5 years of related experience (education can substitute for work experience) in project management, data analysis for the pharmaceutical/healthcare industry 
• Demonstrated advanced level knowledge of Excel, Access and other monitoring tools
• Previous client-facing experience

• Curious, data driven analytical thinker
• High degree of 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
• 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
• Ability to create and motivate a team around project deliverables
• Working proficiency in English

Get to know Labcorp Drug Development 
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations.
Here, you can join our more than 75,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives.

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.

We encourage all to apply

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