Description review

Clinical Data Manager II- QC Specialist

Cytel · India · back to the listing

HR standards

47/100

poor

Title ↔ description

59/100

needs work

Reads as

QA Engineer

99% confident

What this role officially is

software tester — ESCO, the EU occupation classification

Software testers perform software tests. They may also plan and design them. They may also debug and repair software although this mainly corresponds to designers and developers. They ensure that applications function properly before delivering them to internal and external clients.

Also known as: application software tester, unit tester, application tester, software application tester, tester, module tester

How others title the same work

Large employers

Senior Software Quality Engineer Adobe
Distributed Systems Testing Software Engineer, Python / Go Canonical
Ubuntu Linux Kernel Test Engineer Canonical
Distributed Systems Testing Software Engineer, Python / Go Canonical Ltd.
Ubuntu Linux Kernel Test Engineer Canonical Ltd.

Startups

Software Engineer, QA & Test Automation AviaryAI

What the listing never says

No section describes what the person would actually do. Scope clarity
No pay range published. Candidates cannot tell whether applying is worth their time. Pay transparency
No location or timezone policy stated, so a candidate cannot tell where they may work from. Scope clarity

The listing, marked up

Nothing in the wording of this listing tripped a check. The scores above still judge how complete and coherent it is.

The QC Specialist is responsible for planning, executing, and documenting Testing activities for EDC and other systems. This role ensures that systems are tested and programmed to specification, supporting regulatory requirements and high-quality clinical trial data collection. The QC Specialist works closely with Data Management, Database Development, and external partners to verify that system builds meet specification expectations prior to study deployment. and programmed to specification, supporting regulatory requirements and high-quality clinical trial data collection, and external partners to verify that system builds meet specification expectations prior to study deployment.

Originally posted on Himalayas