IQVIA
10+ Vega Building Systems Interview Questions and Answers
Q1. Adverse events and reconciliation and other flow in clinical data management
Adverse events and reconciliation are important aspects of clinical data management.
Adverse events must be reported and documented accurately.
Reconciliation involves comparing data from different sources to ensure consistency.
Flow in clinical data management refers to the movement of data through various stages of the clinical trial process.
Effective management of adverse events and reconciliation can improve data quality and patient safety.
Q2. Day-to-day life of a Data manager
A data manager's day-to-day life involves managing and analyzing data, ensuring data quality, and collaborating with other teams.
Managing and organizing data sets
Ensuring data quality and accuracy
Collaborating with other teams to ensure data is being used effectively
Analyzing data to identify trends and patterns
Creating reports and visualizations to communicate findings
Staying up-to-date with industry trends and advancements in technology
Q3. General activities and routine process in cdm
CDM involves data collection, cleaning, validation, and transformation for clinical trials.
Collecting and organizing data from various sources
Cleaning and validating data to ensure accuracy and completeness
Transforming data into a standardized format for analysis
Creating and maintaining data dictionaries and data management plans
Performing quality control checks on data
Generating reports and data listings for clinical trial teams
Q4. how do you do vendor data reconciliation
Vendor data reconciliation involves comparing and matching data from different sources to ensure accuracy and consistency.
Gather data from vendors and internal systems
Compare data fields such as patient demographics, procedures, and charges
Identify discrepancies and investigate root causes
Resolve discrepancies through communication with vendors and data validation
Document reconciliation process and outcomes
Q5. Brief description of all phases of CDM process
CDM process involves study setup, data collection, data cleaning, database lock, and submission.
Study setup: Defining data collection tools, database structure, and data validation rules.
Data collection: Gathering patient data through case report forms, electronic health records, etc.
Data cleaning: Identifying and resolving discrepancies, errors, and missing data.
Database lock: Finalizing the database to prevent further changes to the data.
Submission: Preparing and submitting...read more
Q6. What is clinical data management
Clinical data management involves collecting, cleaning, and analyzing data from clinical trials and studies to ensure accuracy and compliance.
Involves collecting, cleaning, and analyzing data from clinical trials and studies
Ensures data accuracy and compliance with regulations
Helps in maintaining quality and integrity of clinical data
Uses specialized software and tools for data management
Plays a crucial role in drug development and healthcare decision-making
Q7. what is query management
Query management involves handling and resolving data discrepancies or issues in a database or system.
Identifying discrepancies or errors in data
Creating queries to address the issues
Communicating with relevant stakeholders for resolution
Tracking and documenting the resolution process
Ensuring data integrity and accuracy
Q8. Overview of CDM process
CDM process involves collecting, cleaning, and managing clinical trial data to ensure accuracy and completeness.
CDM process starts with designing a database to collect data
Data is then collected from various sources and cleaned to remove errors and inconsistencies
Data is then transformed and loaded into the database
Data is validated to ensure accuracy and completeness
Queries and reports are generated to analyze the data
CDM process also involves ensuring compliance with regula...read more
Q9. Details about SAE reconciliation
SAE reconciliation involves comparing serious adverse events reported in clinical trials with data from other sources to ensure accuracy.
SAE reconciliation is a crucial step in clinical data management to ensure patient safety and data integrity
It involves comparing SAEs reported in clinical trial data with other sources such as medical records, lab reports, and patient diaries
Any discrepancies found during reconciliation must be resolved through thorough investigation and do...read more
Q10. Types of query reports in Rave
Query reports in Rave help identify data discrepancies and ensure data quality.
Types of query reports in Rave include Open Query Report, Closed Query Report, and Query Aging Report.
Open Query Report displays all unresolved queries in the system.
Closed Query Report shows all resolved queries.
Query Aging Report provides information on the age of queries in the system.
Q11. Difference between AE and SAE
AE refers to any adverse event, while SAE refers to a serious adverse event.
AE can be any undesirable experience associated with the use of a medical product, whether or not considered related to the product.
SAE is a specific type of AE that results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, or is a congenital anomaly/birth defect.
Examples of AEs inc...read more
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