Clinical Trial Data Analyst
6 days ago
Clinical Trial Data Analyst (Global Monitor)
This role is responsible for ensuring that clinical studies' laboratory data is on track by consulting an internal dashboard. If the data is not on track, the role will investigate why and share insights with study Project Managers to rectify and prevent issues.
The Clinical Trial Data Analyst (Global Monitor) will create and maintain the Global Monitoring plan for assigned studies, coordinate the work of Client Coordinator Specialists, Global Monitoring Center, and Regional Study Coordinators, and ensure regular communication with Global Study Managers or Global Study Leads.
- 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 assigned studies to identify issues and ensure risks are proactively addressed.
- Extract information from multiple data sources, converting raw data into meaningful and actionable insights, and present key findings to stakeholders.
- Accountable for the monitoring and reporting of clinical study laboratory metrics on both a monthly and/or ad hoc basis.
- Liaise with Developers to ensure the development of monitoring tools is 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.
- Escalate issues, highlight trends, and liaise closely with Global Study Manager or Global Study Lead throughout the life of the study to ensure monitoring is appropriate.
- Support Risk Management Plan creation and ongoing maintenance through monitoring and analysis.
- Comply with the Central Laboratory Global Project Management strategy.
- Support a culture of continuous improvement, quality, and productivity.
- 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.
- Curious, data-driven analytical thinker.
- Big picture thinker who suggests changes to process, identifies risks, and potential opportunities for data improvement.
- 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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