Job Description:

Introducing Global Clinical Data Integration (GCDI): Transforming clinical data management in Latin America. With a focus on streamlining information, our department collects, cleans, transforms, and archives clinical data, ensuring high quality and compliance. As a new addition to the region, we intend to enhance efficiency and leverage local information across departments to drive innovation and deliver value across clinical trials, data management standards, and technology platforms.

Our Clinical teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards.

CDT Analyst

Responsabilities:

• Execute and document validation activities to uphold data quality and system integrity for standard and study-specific test cases, including recording test data and results and preparing validation summary reports.

• Coordinate and conduct UAT testing

• Creation of trial specific test cases

• Develop data integrity and consistency checks across data pipelines, integrations, and automation workflows

• File essential records in the official repository, maintain traceable evidence, and ensure audit-ready documentation

• Develop, review and maintain UAT release documents for trial-based configuration, including any change control documents

Requirements:

• B.A. or B.S. degree or student, preferably in mathematics, science, health care related disciplines, or computer science.

• English proficiency C1

• Familiar with clinical data management systems and platforms

• Familiar with test management solution (e.g., Jira Xray)

• Understands GxP, computer system validation (CSV), and other regulatory guidelines

• Basic knowledge of system development lifecycle management

• Follow good documentation and testing practice

Soft skills:

• Coordination skills to oversee timelines, resources and team deliverables

• Ability to communicate clearly with both technical and non-technical stakeholders and to facilitate communication among team members

• Prioritize work effectively and meet deadlines, maintaining high standards of accuracy and data integrity

Work both independently and collaboratively within diverse teams to achieve common goals

Required Skills:

Accountability, Accountability, Adaptability, Analytical Problem Solving, Automation in Systems Integration, Clinical Data Cleaning, Clinical Data Management, Clinical Documentation, Clinical Trials, Communication, Computer Science, Cross-Cultural Teams, Data Analysis, Data Documentation, Data Entry, Data Integrity, Data Processing, Data Quality, Data Quality Control, Data Reporting, Data Review, Data Validation, Data Visualization, Good Clinical Practice (GCP), Integrity Management {+ 4 more}

Preferred Skills:

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Current Contingent Workers apply HERE:

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Employee Status:

Project Temps (Fixed Term)

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

04/3/2026

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