Associate Specialist, Clinical Data Management - Hybrid

Merck · Rahway, NJ

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BiometricsFull-time$72k–$113kCompany career page

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Role summary

Merck seeks an Associate Clinical Data Management Analyst to support testing and validation of clinical data management systems used in clinical trials. The role involves quality control testing, user acceptance testing, and collaboration with cross-functional teams to ensure compliance with regulatory standards and company procedures.

What they're looking for

Bachelor's degree in Mathematics, Computer Science, Life Sciences, Health Care, Information Systems, or related field
Basic understanding of Software Development Lifecycle (SDLC) and system validation
Strong attention to detail with focus on quality assurance
Proficiency in Microsoft Office (Excel, Word, PowerPoint)
Ability to manage multiple priorities and work independently or collaboratively
Good written and verbal communication skills
Analytical and problem-solving skills

What you'll be doing

Create and execute quality control and user acceptance testing procedures for clinical data management systems
Test and validate Electronic Data Capture systems, electronic diaries, IVRS/IWRS systems, and related technologies
Develop test documentation including test plans, scripts, traceability matrices, and testing evidence
Identify, document, and communicate testing issues to support resolution efforts
Collaborate with clinical data management, programming, and technical teams to ensure requirements are understood and implemented

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