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Clario looking for Study QC Analyst


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Clario looking for Study QC Analyst

For almost 50 years, we have led the way in delivering better clinical evidence with our clinical research data management services. In that time, our technology, expertise and know-how have helped more than 800 new drugs come to market.

Post : Study QC Analyst

Job Description :
• Analyzing project documents from a testing perspective, verifying accuracy and completeness
• Creating test plans, scripts, and cases necessary for testing projects
• Executing test plans, and documenting results
• Managing defect log and tracking issue resolution with project build staff
• Verifying testing fixes and documenting completion of all QC testing
• Reporting testing and reviewing anomalies, as appropriate, to manager or the designated project teams
• Verifying work of other QA Test Analysts to ensure quality deliverables
• Reading, understanding and adhering to organizational Standard Operating Procedures (SOPs), Work Instructions (WIs) and Templates
• Assisting in establishing and enforcing departmental standards
• Participating in the modification of company SOPs related to IVR/IWR Testing
• Working as a mentor to provide guidance to the Associate IRT Study QC Analyst by providing guidance on Trident EUS and Trident ADMIN capabilities
• Working as a mentor to provide guidance to the Associate IRT Study QC Analyst by providing guidance on the structure of the Trident database
• Exploring new opportunities to add value to organization and departmental processes
• Helping others to achieve results
• Performing other duties as assigned
• Performing verification of completed client-requested Data Changes
• Performing verification of completed Maintenance Issues
• Performing verification of client-requested Custom Reports and Data Extracts
• Attending and participating in applicable company sponsored training
• Attending educational workshops and reviewing professional publications
• Benchmarking state-of-the-art practices
• Participating in professional societies
• Keeping informed of changes in the regulatory environment and/or regulatory requirements

Candidate Profile :
•  Bachelor’s degree required, preferably in the Life Sciences, or related field, or equivalent and relevant work experience in a software product development environment.
• 1+ years’ experience carrying out quality assurance and quality control activities.
• Experience working in a team environment where deliverables and timelines must be met.
• Prior testing experience with pharmaceutical related software, preferred
• Strong interpersonal and communication skills, both verbal and written
• Goal oriented
• Ability to make sound judgments
• Superior problem-solving skills
• Ability to manage multiple tasks effectively & efficiently

Additional Information
Location : Pondicherry, Mysore, Bangalore
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : QC
End Date : 30th December, 2022

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