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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