Develop, validate, and maintain SAS programs for clinical study deliverables.
Generate and review Data Validation Listings (DVLs) to ensure data accuracy, completeness, and consistency.
Support the creation and maintenance of clinical data outputs, reports, and listings.
Apply programming best practices, including code optimization, documentation, and quality control.
Collaborate with cross-functional teams including Data Management, Biostatistics, and Clinical Operations.
Utilize SAS macros and SQL programming to automate and streamline processes.
Participate in data review activities and contribute to issue resolution.
Support study milestones and timelines while ensuring adherence to regulatory and company standards.
Required Qualifications: -
Strong proficiency in SAS programming.
Hands-on experience in developing and reviewing Data Validation Listings.
Good understanding of clinical trial data and programming standards.
Working knowledge of SAS Macros and SQL.
Strong analytical, problem-solving, and communication skills.
Demonstrated understanding of programming best practices and quality standards.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Role : Database Engineer / SpecialistA highly skilled Database Specialist with a strong passion for data, database technologies, and modern data architecture. Brings deep expertise in data modelling, schema design, database optimisation, and enterprise data management across relational and NoSQL platforms - designing and ...
... security policies. - Meet defined quality, productivity, and SLA targets. - Identify opportunities to improve data management processes. Required Skills - Data Management - Data Entry and Data Processing - Data Validation and Verification - Data Quality Management - MS Excel and MS Office - Database Management - Data Analysis ...
... Maintenance of Master data & Parts lists - Monitoring of Master Data Quality - Implementation of changes from assembly groups in ERP system and the feature database - Classification of different parts - Supports for common rules & configuration in division - Management of documents and numbering system - Transfer of data ...
... Maintenance of Master data & Parts lists - Monitoring of Master Data Quality - Implementation of changes from assembly groups in ERP system and the feature database - Classification of different parts - Supports for common rules & configuration in division - Management of documents and numbering system - Transfer of data ...
... enterprise resource planning (ERP) software, SAP has evolved to become a market leader in end-to-end business application software and related services for database, analytics, intelligent technologies, and experience management. As a cloud company with two hundred million users and more than one hundred thousand employees ...
... Vault, Storage, PostgreSQL / SQL, Service Bus and Front Door. - Azure AI: Azure AI Foundry / Azure OpenAI production implementation, model deployment, quota management, routing and content filtering. - Multi-Tenant Architecture: Tenant isolation using subscriptions, resource groups, namespaces or database-level isolation. ...
Associate Safety Reporting Specialist at Thermo Fisher Scientific responsible for receiving, preparing, and submitting expedited and periodic safety reports while tracking submissions and supporting regulatory compliance across clinical trial projects. Responsibilities - Receive, prepare, and submit safety reports to applicable ...
... scheduled report distributions for business stakeholders across multiple departments. Integrated reporting solutions with enterprise applications and various database systems, ensuring high performance, data accuracy, and security. Collaborating with business users, analysts, and development teams to gather reporting requirements, ...
... scheduled report distributions for business stakeholders across multiple departments. Integrated reporting solutions with enterprise applications and various database systems, ensuring high performance, data accuracy, and security. Collaborating with business users, analysts, and development teams to gather reporting requirements, ...
... delivery, and database lock - Investigate laboratory data discrepancies and escalate risks and quality concerns appropriately - Partner with Clinical Data Management, Clinical Operations, and external providers to deliver activities on schedule Requirements - Bachelor's degree in science, health, data management, mathematics, ...
Associate Safety Reporting Specialist at Thermo Fisher Scientific responsible for receiving, preparing, and submitting expedited and periodic safety reports while tracking submissions and supporting regulatory compliance across clinical trial projects. Responsibilities - Receive, prepare, and submit safety reports to applicable ...