HCL Tech- Hiring For UAT Testing Clinical Trail Management

4 days ago

Hyderabad, Telangana, India HCLTech Full time ₹ 10,000 - ₹ 25,000 per year

Dear Talent,

Greetings from HCL Technologies

We are pleased to inform you that we currently have opening for UAT Testing

Skill Required-

UAT Testing, Clinical Trail Management Systems (CTMS), Clinical Data Management (CDM), ALM, UFT, JIRA

Location Hyderabad

Experience 5-10 years

Notice: Immediate- 90 Days

Please revert with the below details along with your Update CV.

Name:

Contact Number:

Email ID:

Total Exp:

Relevant Exp in UAT:

Relevant Exp in Clinical Trail Management/ Clinical Data Management systems:

Current CTC:

Expected CTC:

Current Org:

Current Location:

Preferred location:

Notice Period:

EX-HCL Employee: Yes/No

If yes SAP code-HCL:

Available for F2F Interivew: Yes/No

Available Date:

Available Timing (10:00 AM- 12:00 PM):

Skill set:

Primary Skill Planning, executing, and managing UAT activities for applications supporting clinical operations, UAT Testing, Clinical Trail Management Systems (CTMS), Clinical Data Management (CDM), Electronic Data Capture (EDC), patient randomization, monitoring, and trial documentation, Functional & UAT Testing, Experience with ALM, UFT, JIRA

Secondary Skill Safety, Regulatory, Pre-clinical, R&D, Discovery, Argus, Veeva Clinical & Safety RIMS.

Roles and Responsibilities

Must Have

  • 4–8+ 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, eTMF, IRT/IWRS, eCOA/ePRO, 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 eTMF 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 InForm, Veeva CTMS, Medrio, Oracle Siebel CTMS, Veeva eTMF, 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.

Interested Candidate share your resume to

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