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Job Description: Must-Have Skillset 5-7 years of experience as BA with 4 years of minimum experience in Clinical Trial Domain / Clinical Data as BAStrong experience in clinical trials, EDC/RAVE Data, and clinical data platformsExpertise in requirements gathering, gap analysis, and functional documentationBasic understanding and hands-on experience on Oracle SQL, Table Structure Basics.Proficiency in tools like Excel, JIRA, ConfluenceKnowledge and hands-on experience on Oracle SQL, Table Structure Basics.Strong knowledge on SDLCGood-to-Have Skillset Experience with data transformation rules, source-to-target mapping, and vendor file validationKnowledge of technical and grammatical editingFamiliarity with audit support and compliance documentationAbility to learn and use modelling languages when / where required Key Responsibilities Gathering of initial Business Case requirements & other pre-project activities (e.g., high-level requirements, project scope, objectives)Perform requirements gathering and analysis to provide high quality and detailed requirements, ensuring the closest involvement with, and agreement from, the user communityFacilitate UAT planning, execution, and documentation for study rolloutsCollaborate with internal teams and external clients to resolve data issuesResolve conflicting end-user requirementsFollow IQVIA Systems Development Life Cycle (SDLC) and Computer System Validation (CSV) procedures, as appropriateCollaborate with the Lead User, or delegated member of the applicable business group, to create a User Requirements Specification documentCollaborate with the Development group to create a Functional Specification (FS) documentAssist with process modelling to clarify business requirements, and to enhance or re-engineer business processes, prior to, or in parallel with, solution design and implementation, as necessaryAs needed, assist with the review of the Performance Qualification (PQ) document(s) prior to authorization and execution, to ensure that it incorporates previously captured requirements, and includes tests or test steps that explicitly address each identified user requirementCollaborate with Global IT Solutions functional groups by adhering to established processes to ensure that business requirements are delivered through successful project implementation of optimal, cost-effective solutionsCollaborate with developers and testers to ensure adherence to business requirements and UI design specificationsDevelop training and support programs for global technology and process implementations, as neededProvide timely updates, issue summaries, and follow-ups to stakeholdersRecommend process improvements and contribute to digital transformation initiativesEnsure compliance with regulatory standards and support audit readiness MINIMUM REQUIRED EDUCATION AND EXPERIENCE BE, bachelors or masters Degree, Clinical Information Management or equivalent qualifications (B. Pharma & M. Pharma). Job Description: Must-Have Skillset 5-7 years of experience as BA with 4 years of minimum experience in Clinical Trial Domain / Clinical Data as BAStrong experience in clinical trials, EDC/RAVE Data, and clinical data platformsExpertise in requirements gathering, gap analysis, and functional documentationBasic understanding and hands-on experience on Oracle SQL, Table Structure Basics.Proficiency in tools like Excel, JIRA, ConfluenceKnowledge and hands-on experience on Oracle SQL, Table Structure Basics.Strong knowledge on SDLCGood-to-Have Skillset Experience with data transformation rules, source-to-target mapping, and vendor file validationKnowledge of technical and grammatical editingFamiliarity with audit support and compliance documentationAbility to learn and use modelling languages when / where required Key Responsibilities Gathering of initial Business Case requirements & other pre-project activities (e.g., high-level requirements, project scope, objectives)Perform requirements gathering and analysis to provide high quality and detailed requirements, ensuring the closest involvement with, and agreement from, the user communityFacilitate UAT planning, execution, and documentation for study rolloutsCollaborate with internal teams and external clients to resolve data issuesResolve conflicting end-user requirementsFollow IQVIA Systems Development Life Cycle (SDLC) and Computer System Validation (CSV) procedures, as appropriateCollaborate with the Lead User, or delegated member of the applicable business group, to create a User Requirements Specification documentCollaborate with the Development group to create a Functional Specification (FS) documentAssist with process modelling to clarify business requirements, and to enhance or re-engineer business processes, prior to, or in parallel with, solution design and implementation, as necessaryAs needed, assist with the review of the Performance Qualification (PQ) document(s) prior to authorization and execution, to ensure that
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