Please mention DailyRemote when applying
AI Summary
The Validation Analyst is responsible for developing and executing test scripts to ensure the safety and integrity of clinical trial software. This includes documenting defects, verifying configuration settings, and providing cross-functional support for data quality reports.
Company Information
Clinical Ink is the global life science company that brings data, technology, and patient science together to unlock clinical discovery. Our deep therapeutic-area expertise, coupled with Direct Data Capture, eCOA, eConsent, telehealth, neurocognitive testing, and digital biomarkers advancement, drive the industry standard for data precision and usher in a new generation of clinical trials. With offices in the United States and Denmark, Clinical Ink is rewriting the clinical development experience.
Job Description
Clinical Ink is seeking a Validation Analyst to join our Project Quality team based remotely across the United States! This individual will contribute to developing and overseeing the execution of test scripts for clinical trial software. The Validation Analyst's responsibilities include:
Clinical Ink is the global life science company that brings data, technology, and patient science together to unlock clinical discovery. Our deep therapeutic-area expertise, coupled with Direct Data Capture, eCOA, eConsent, telehealth, neurocognitive testing, and digital biomarkers advancement, drive the industry standard for data precision and usher in a new generation of clinical trials. With offices in the United States and Denmark, Clinical Ink is rewriting the clinical development experience.
Job Description
Clinical Ink is seeking a Validation Analyst to join our Project Quality team based remotely across the United States! This individual will contribute to developing and overseeing the execution of test scripts for clinical trial software. The Validation Analyst's responsibilities include:
- Develop and oversee the execution of testing scripts
- Ensure the correct functioning of clinical trial software with focus on patient safety and integrity of clinical study data by:
- Ensuring requirements are clear, testable, and consistent with the clinical trial
protocol - Proofreading requirements for spelling and congruency with clinical trial protocol
- Scripting and/or conducting protocol/project specific testing to ensure fulfillment of study design, build, and implementation requirements
- Documenting testing in accordance with applicable process and procedures
- Executing qualification testing on section build requirements
- Executing qualification testing on form design requirements
- Documenting defects and tracking to resolution
- Verifying approved study-specific configuration settings
- Ensuring requirements are clear, testable, and consistent with the clinical trial
- As required, assist with the execution of platform testing
- Provide cross-functional support to Data Quality, as needed, including:
- Verify and validate data reports and exports
- Verify data clarifications
- Perform other related duties as assigned
Qualifications
- Associates degree or relevant experience
- Strong written/verbal communication skills; ability to communicate with personnel at various levels
- Exceptional computer skills; proficiency with Microsoft Word, Excel, etc.
- Detail-oriented and analytical reasoning skills
- Sense of ownership and proactive approach to work
- Effective prioritization, time management, and organizational skills
Additional Information
Clinical ink is an equal opportunity employer and does not discriminate against otherwise qualified applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or handicap, or veteran status.
www.clinicalink.com
Automatically Apply to the Best Remote Jobs
Stop the endless job search. Our AI finds and applies to the best jobs for you.
