Senior Clinical Data Specialist

2 days ago

Hyderabad, Telangana, India beBeeClinicalResearch Full time ₹ 1,00,00,000 - ₹ 1,50,00,000

We are seeking a talented individual to fill the role of Clinical Research Associate. This position involves performing user acceptance testing for clinical forms, database edit checks, and reports/listings.

  • Applicants must possess a Bachelor's degree in Life Sciences or Computer Science.
  • A minimum of 8 years of experience in clinical data testing and validation is required.
Benefits:
  • The opportunity to work with a global technology company that helps enterprises reimagine their businesses for the digital age.
  • A chance to contribute to our mission of delivering exceptional technology solutions.

The ideal candidate will have strong experience with clinical study setup and CDMS platforms, as well as CTMS. They will be able to review edit check specifications, write, and execute UAT scripts. Additionally, they will conduct quality control on metadata listings and peer review of programming checks.

The selected candidate will be expected to ensure consistent use of clinical data standards across programs and repositories. They will also work with clinical data management systems to validate database builds and data flows. Furthermore, they will ensure compliance with regulatory requirements and internal SOPs.

Key Responsibilities:
  • Perform user acceptance testing (UAT) for clinical forms, database edit checks, and reports/listings.
  • Test clinical study setup configurations, including protocol parameters, visit schedules, and form designs.
  • Validate external data acquisition and ensure accurate processing.
  • Collaborate with clinical data scientists and study data managers to understand study scope and expectations.
  • Review edit check specifications, write, and execute UAT scripts.
  • Conduct quality control on metadata listings and peer review of programming checks.
  • Support automation tool validation and standardization of test scripts.
  • Ensure consistent use of clinical data standards across programs and repositories.
  • Work with clinical data management systems to validate database builds and data flows.
  • Ensure compliance with regulatory requirements and internal SOPs.
  • Document and share study-related testing deliverables and lessons learned.

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