CDT Analyst II

MSD Malaysia; Warszawa; Hybrid; PLN 120,000 - 180,000; Full time

Job summary

Merck & Co., Inc. seeks a QA/Test Analyst to execute standard and trial-specific test scripts, document results, and develop test plans. The role covers SDLC management, system validation, and data management within GDMS applications in a hybrid environment.

You will create and modify test scripts, coordinate testing activities, triage issues from UAT, and mentor junior staff. A BS in science or CS and 2+ years in clinical data management or software testing are preferred; visa sponsorship may

Qualifications

• 2+ years SDLC management and system validation knowledge.
• Database design and development knowledge.
• Knowledge of the clinical development process.
• Knowledge of database structures and tools to manage, extract and report data.

Responsibilities

• Execute standard and trial-specific test scripts; record data and results.
• Create and modify test scripts as needed.
• Develop test plans and test summaries for clinical trials.
• Coordinate and facilitate testing activities for the tested tool/system.
• Triaging and categorizing issues identified during UAT.
• Mentor new/less experienced staff in the department.

Skills

Application Testing

Clinical Data Management

Database Development

Database Queries

Data Validation

Data Visualization

EDC

Functional Testing

PL/SQL

Scripting

Software Analysis

Software Testing Tools

System Implementations

System Validation

Education

Bachelor's degree (healthcare/biotech/math/science/CS)

Tools

Test Tools

Database Tools

Job description

Job Description

Position overview: 50% Perform execution of standard and trial specific test scripts and record test data and test results; Edit check Matrix testing: - Creation of and the execution of standard and trial specific test scripts - Develops knowledge in programming and system analysis and testing within GDMS applications - Ensures all testing documentation is stored in electronic trial master file - May support the testing of tools and applications; including creating Test Plan, Test Scripts and execution of test scripts 15% Responsible for the creation of Test Plans and Test Summary documentation for a clinical trial 5% Responsible for the creation/modification of standard and trial specific test scripts 10% Responsible for the facilitation and coordination of testing activities related to the tool/system being tested 10% Responsible for the triaging and categorization of issues identified during UAT 5% May be assigned to support special projects within the GCDI functions 5% May be assigned as a mentor to new and less experienced staff in the department

Education:

A B.A. or B.S. degree, preferably in healthcare-related discipline, biotechnology, mathematics, science or computer science; or relevant skills and experience.

Knowledge and Skills:

• 1. 2+ Years of System Development Lifecycle Management / system validation knowledge
• 2. Database design and development knowledge.
• 3. An overall working knowledge of the clinical development process.
• 4. Knowledge of database structures and available tools to manage, extract, and report data is preferred.
• 5. Exceptional communication skills (oral and written) with the ability to communicate with both the technical and business areas.
• 6. Exceptional organizational and problem-solving skills.
• 7. Ability to work cross-functionally and as part of a team.
• 8. Able to work under pressure and change environment with flexibility.

Required Skills:

• Application Testing
• Clinical Data Management
• Database Development
• Database Queries
• Data Validation
• Data Visualization
• Electronic Data Capture (EDC)
• Functional Testing
• PL/SQL (Programming Language)
• Scripting
• Software Analysis
• Software Testing Tools
• System Implementations
• System Validation

Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift: Valid Driving License: Hazardous Material(s):

Job Posting End Date: 09/30/2026

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.