Reporting Associate
Core
Drafting and finalizing nonclinical study reports for GLP-regulated studies, incorporating contributions and ensuring data accuracy.
Role type
Associate clinical reporting specialist
Builds
Nonclinical study reports and data tables
Domain
Life sciences / Clinical research / GLP compliance
Required skills
Report drafting, data table preparation, quality assurance inspection, protocol adherence, client interaction, task prioritization
Preferred skills
Microsoft Office proficiency (Word, Excel, Acrobat), data analysis, multi-tasking
Technologies
Microsoft Word, Microsoft Excel, Adobe Acrobat
Responsibilities
Drafting and finalizing nonclinical study reports, preparing study reports using protocol details, addressing quality assurance inspection items, reviewing data tables for accuracy, managing full study workload with complex designs
Seniority
Entry-level / Associate
