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10+ Vega Building Systems Interview Questions and Answers

Updated 12 Nov 2024
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Q1. Adverse events and reconciliation and other flow in clinical data management

Ans.

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.

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Q2. Day-to-day life of a Data manager

Ans.

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

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Q3. General activities and routine process in cdm

Ans.

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

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Q4. how do you do vendor data reconciliation

Ans.

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

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Q5. Brief description of all phases of CDM process

Ans.

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

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Q6. What is clinical data management

Ans.

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

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Q7. what is query management

Ans.

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

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Q8. Overview of CDM process

Ans.

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

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Q9. Details about SAE reconciliation

Ans.

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

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Q10. Types of query reports in Rave

Ans.

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.

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Q11. Difference between AE and SAE

Ans.

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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Interview Process at Vega Building Systems

based on 11 interviews in the last 1 year
1 Interview rounds
Technical Round
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