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Software tester

Software tester

HCLTechHyderabad, Andhra Pradesh, India
6 days ago
Job description

Job Profile : UAT Tester - CTMS & CDM applications

Location : Hyderabad

Notice period : immediate to 60 days

Mandatory Requirements : Clinical Systems, Safety Systems, 21 CFR part 11, GAMP 5, ICH, EMEA, MHRA regulations

Roles and Responsibilities

Must Have

4 to 8+ years of experience in IT testing / validation, with 2–4+ years in clinical trial systems.

Collaborate with Clinical Operations, Data Management, Biostatistics, and IT teams to gather UAT requirements.

Develop UAT strategy, test plans, test cases, and traceability matrices mapped to URS (User Requirements).

Execute UAT test scripts for CTMS, EDC, e TMF, IRT / IWRS, e COA / e PRO, and integrations with Safety and Regulatory systems.

Validate workflows such as :

Site / investigator setup and activation

Subject enrollment, randomization, drug dispensing, and visit scheduling

Data entry, query management, and monitoring

Document upload, versioning, and e TMF compliance

Reporting and dashboard validation

Perform regression testing for upgrades, patches, and system integrations.

Log defects, participate in triage, and track to closure with IT / vendors.

Ensure compliance with ICH-GCP, GAMP 5, 21 CFR Part 11, GDPR, and other regulatory standards.

Support end-user training, readiness checks, and sign-off for system release.

Provide UAT summary reports and contribute to release go / no-go decisions.

Maintain UAT documentation for audits and regulatory inspections.

Support process improvements, automation, and efficiency in UAT cycles.

Good to Have (secondary skills)

Hands-on experience with Clinical applications (e.g., Medidata Rave, Oracle In Form, Veeva CTMS, Medrio, Oracle Siebel CTMS, Veeva e TMF, IRT / IWRS systems).

Knowledge of clinical trial processes (site initiation, subject enrollment, monitoring, data management, trial closure).

Familiarity with UAT methodology, SDLC, and CSV (Computer System Validation) practices.

Strong knowledge of ICH-GCP, FDA, EMA, and MHRA clinical trial regulations.

Proficiency in defect tracking tools (e.g., JIRA, HP ALM, Veeva QMS).

Excellent communication, analytical, and problem-solving skills.

Ability to work cross-functionally with Clinical, QA, Data, and IT teams.

Communication

Immaculate communication and handles multiple clients / projects

Works in Consulting capacity

Best Regards,

Aditi Agarwal

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Software Tester • Hyderabad, Andhra Pradesh, India

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