Reporting Associate

Overview

In this role you will draft and finalize nonclinical study reports and manage a multi-study workload. You will work within the Global Reporting Solutions team to produce accurate reports that follow protocols and GLP standards. You will interact with clients and collaborate with cross-functional partners, supported by comprehensive training. This position combines scientific reporting with data handling in a hybrid setup, contributing to Labcorp’s mission to advance health outcomes.

Pay / Benefits

• competitive salary
• comprehensive benefits package including health coverage
• contributory pension
• career development opportunities
• CARE culture with wellbeing programs
• hybrid and flexible working

Responsibilities

• Draft and finalize nonclinical study reports
• Use software tools for word processing, spreadsheets, tables, collaboration, and database applications
• Prepare study reports per protocol details
• Incorporate protocol amendments and certificates of analysis into drafts
• Address quality assurance items on GLP-regulated studies
• Draft and quality check data tables; verify data accuracy
• Review data tables for correctness
• Interact with clients
• Manage a full workload with complex study designs and prioritize tasks

Key requirements

• BSc degree
• Relevant experience may substitute for academic qualifications
• Proficiency with office software (Word, Excel) and Adobe Acrobat
• Strong analytical and problem-solving skills
• Effective written and verbal communication
• Strong attention to detail and data accuracy
• Ability to manage multiple priorities and meet deadlines

• effective written and verbal communication
• attention to detail
• time management / prioritization
• Microsoft Word
• Microsoft Excel
• Adobe Acrobat

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