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) - 1 year contract.
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
* Utilize analytics/visualizations to review study laboratory data for your assigned studies to identify issues and to ensure risks are proactively addressed.
* Extract 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 and the Study Design Lead).
* 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 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
What we’re looking for
* 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
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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