Reporting Associate
Core
Drafting and finalizing nonclinical study reports for GLP-regulated studies, incorporating contributions and ensuring data accuracy.
Role type
Reporting Associate (Clinical Research)
Builds
Nonclinical study reports and data tables
Domain
Life Sciences / Clinical Research / GLP Compliance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Report drafting, data table preparation, quality assurance inspection, protocol adherence, client interaction, task prioritization
Preferred skills
Advanced Microsoft Office (Word, Excel, Acrobat), analytical problem-solving, attention to detail
Technologies
Microsoft Word, Microsoft Excel, Adobe Acrobat
Responsibilities
Drafting and finalizing nonclinical study reports, preparing study reports using protocol details, incorporating contributions into draft reports, addressing quality assurance inspection items on GLP-regulated studies, reviewing data tables for accuracy, managing a full study workload with complex study designs
Seniority
Entry to Mid-level, full training provided