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Study QC Analyst

1.00 to 3.00 Years   Bangalore   21 Jan, 2022
BioClinica
Job LocationBangalore
EducationNot Mentioned
SalaryNot Disclosed
IndustryFMCG / F&B
Functional AreaStatistics / Analytics
EmploymentTypeFull-time

Job Description

Primary ResponsibilitiesPerform study-specific QC Testing of IRT programs by:

  • 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
Maintains Quality Service and Departmental Standards by
  • 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
Secondary ResponsibilitiesContributes to team effort by
  • 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
Maintains Professional and Technical Knowledge by
  • 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
QualificationsEducation:
  • Bachelor s degree required, preferably in the Life Sciences, or related field, or equivalent and relevant work experience in a software product development environment.
Experience:
  • 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
Additional skill set:
  • 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
Working conditionsTravel: 0-10%Lifting: 0-25 lbs.Other: Computer work for long periods of timeThis JOB description should not be deemed all-inclusive. Additional requirements and expectations may be assigned. At all times, employees are expected to adhere to company policies and company SOPs.EEO StatementBioclinica is an equal opportunity employer. Bioclinica evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.Collaboration, Continuous Learning, Critical Thinking, Organizational Awareness, Results Orientation, Service Orientation,

Keyskills :
software product developmentstandard operating procedureslife sciencescustom reportsquality controlproblem solvingissue resolutionquality assurancecritical thinkingwork instructionsstatements of work sow

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