Clinical Data Validation & QA Analyst

MSD UK; Rahway (NJ); Hybrid; USD 72,000 - 113,000; Full time

Benefits offered by this job

Medical

Dental

Vision

401(k)

Paid holidays

Vacation

Sick days

Hybrid work

Job summary

Merck & Co., Inc. in Rahway, NJ is seeking an Associate Clinical Data Management Analyst to support testing and validation of clinical data management systems used in trials. This role emphasizes SDLC compliance and GCP guidelines with collaboration across cross-functional teams.

The position requires knowledge of EDC systems, data management concepts, and strong problem-solving, communication, and data documentation skills. Eligible for annual bonus and benefits. Hybrid work arrangement.

Qualifications

• Basic understanding of SDLC and system validation.
• Strong attention to detail and quality.
• Good written and verbal communication skills.
• Ability to work independently and with cross-functional teams.
• Proficiency in Microsoft Office (Excel, Word, PowerPoint).
• Ability to manage multiple priorities in a dynamic environment.

Responsibilities

• Support QC Testing and UAT procedures for clinical data management systems.
• Participate in testing/validation of EDC systems and related technologies.
• Create, review and maintain test documentation (plans, scripts, traceability).
• Collaborate with CDM, Programming, Standards, and technical teams.
• Review database configurations, edit checks, and data transfers.
• Identify, document and communicate testing issues and resolutions.
• Contribute to SDLC compliance and regulatory expectations.
• Develop knowledge of CDM processes and validation methodologies.
• Participate in departmental initiatives and continuous improvement.

Skills

Coordination

Adaptability

Analytical thinking

Computer science

Cross-functional PM

Data documentation

Data validation

GCP

SDLC

Education

B.S. / B.A. in Math, CS, Life Sciences, Healthcare, IS

Tools

SQL

Python

Automation tools

Generative AI

Job description

Merck & Co., Inc. in Rahway, NJ is seeking an Associate Clinical Data Management Analyst to support testing and validation of clinical data management systems used in trials. This role emphasizes SDLC compliance and GCP guidelines with collaboration across cross-functional teams.

The position requires knowledge of EDC systems, data management concepts, and strong problem-solving, communication, and data documentation skills. Eligible for annual bonus and benefits. Hybrid work arrangement.