SIRO Clinpharm Pvt. Ltd. | Principal Programmer Veeva EDC
2 weeks ago
- Create eCRF specifications, design, develop and validate clinical trial setup process
- Create edit check specifications and setup edit checks at trial level
- Implement UAT scripts to test the setup of the clinical study
- Setup different instances of study URL(eg: UAT, production, testing etc.,)
- Setup and configure user accounts for study teams
- Setup and manage blinded and unblinded study configurations
- Be the SME for all EDC database related activities
- Setup, configure, validate and integrate other modules within the EDC ecosystem such as coding, integration of IRT, safety system, local labs etc.,
- Understanding of when custom functions are required within EDC systems
- Ability to troubleshoot database setup as per study needs
- Prepare, test and implement post production changes as per study needs
- Partner with appropriate team members to establish technology standards and governance models
- Oversee system delivery life cycle in collaboration with appropriate partners including Clinical Operations, Clinical Supplies, IT, and Quality organizations
- Be a primary change agent to ensure adoption of new capabilities and business process
- Be the contact for Clinical Technology vendors to ensure established milestones are met with the highest degree of quality.
- Work with leaders to resolve issues affecting the delivery of clinical trials
- Work closely with data engineers and data management programmers on study level integrations and deliveries
- Lead technology vendor oversight activities.
- Partner with appropriate team members, technology vendors, and CRO partners to avoid and resolve risks.
- Confirm archival and inspection readiness of all Clinical Technology Trial Master File (TMF) documents
- Participate in preparing function for submission readiness and may represent Clinical Information Operations (CIO) group in a formal inspection or audit.
- Track study deliverables and evaluate study metrics to mitigate risk for major data management deliverables.
- Adaptable to new ways of working using technology to accelerate clinical trial setup
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Clinical Data Programmer for Veeva CDB
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India SIRO Clinpharm Pvt. Ltd. Full timeJob Description:SIRO Clinpharm Pvt. Ltd. is seeking a skilled Clinical Data Programmer to join our team. The successful candidate will have expertise in Veeva Clinical Query Language (CQL) and data ingestion into Veeva CDB.About the Role:The Clinical Data Programmer will be responsible for developing custom listings based on customer data cleaning...
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Clinical Data Specialist
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Senior Clinical Systems Engineer
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India SIRO Clinpharm Pvt. Ltd. Full timeJob OverviewSiro Clinpharm Pvt. Ltd., a leading Contract Research Organization (CRO), is seeking an experienced Senior Clinical Systems Engineer to join our team. In this role, you will be responsible for designing, developing, and validating clinical trial setup processes using EDC database systems.
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india SIRO Clinpharm Pvt. Ltd. Full timeRole & Responsibility: Develop custom listings based on customer data cleaning requirements using Veeva Clinical Query Language CQL (SQL-based language). Configure and support data ingestions (imports) into Veeva CDB Collaborate with clinical data providers (Central Laboratories, ECG, eCOA, IRT, etc.) to receive data and test the transfer based on...
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Principal Programmer Veeva EDC
6 months ago
India SIRO Clinpharm Pvt. Ltd. Full timeCreate eCRF specifications, design, develop and validate clinical trial setup processCreate edit check specifications and setup edit checks at trial levelImplement UAT scripts to test the setup of the clinical studySetup different instances of study URL(eg: UAT, production, testing etc.,)Setup and configure user accounts for study teamsSetup and manage...
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Principal Programmer Veeva EDC
6 months ago
India SIRO Clinpharm Pvt. Ltd. Full timeCreate eCRF specifications, design, develop and validate clinical trial setup process Create edit check specifications and setup edit checks at trial level Implement UAT scripts to test the setup of the clinical study Setup different instances of study URL(eg: UAT, production, testing etc.,) Setup and configure user accounts for study teams Setup and manage...
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india SIRO Clinpharm Pvt. Ltd. Full timeSkills needed - Veeva Vault Rest API for fetching data with 3 years of experience; Well versed in AWS tools , will be good if AWS architect certified; GitHub; GitAction; Experience in deploying Data Pipelines.Soft Skills - Good communication skills; Requirement gathering; Aliasing with clientUnderstanding of tools - Jira; Confluence
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Veeva CDB Listing Programmer
5 months ago
India SIRO Clinpharm Pvt. Ltd. Full timeRole & Responsibility: Develop custom listings based on customer data cleaning requirements using Veeva Clinical Query Language CQL (SQL-based language).Configure and support data ingestions (imports) into Veeva CDBCollaborate with clinical data providers (Central Laboratories, ECG, eCOA, IRT, etc.) to receive data and test the transfer based on requirements...
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Veeva CDB Listing Programmer
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India SIRO Clinpharm Pvt. Ltd. Full timeRole & Responsibility: Develop custom listings based on customer data cleaning requirements using Veeva Clinical Query Language CQL (SQL-based language). Configure and support data ingestions (imports) into Veeva CDB Collaborate with clinical data providers (Central Laboratories, ECG, eCOA, IRT, etc.) to receive data and test the transfer based on...
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Veeva CDB Listing Programmer
5 months ago
India SIRO Clinpharm Pvt. Ltd. Full timeRole & Responsibility: Develop custom listings based on customer data cleaning requirements using Veeva Clinical Query Language CQL (SQL-based language). Configure and support data ingestions (imports) into Veeva CDB Collaborate with clinical data providers (Central Laboratories, ECG, eCOA, IRT, etc.) to receive data and test the transfer based on...
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Veeva Programmer
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India Atorus Research Inc. Full time**Veeva Programmer** remote from anywhere in India Full-time or Contract - At least 2 to 3 years of hands-on experience as an EDC programming specific to Veeva CDMS - **Must have experience with Veeva CDMS.** - **Must have experience in eCRF development, Rules Programming, and study deployment activities.**: - **Deep knowledge of Veeva study configuration...
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Senior Integration Architect
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India SIRO Clinpharm Pvt. Ltd. Full timeJob OverviewSIRO Clinpharm Pvt. Ltd. is seeking a skilled Lead Statistical Data Analyst to join our team. As a critical member of our study teams, you will be responsible for delivering high-quality statistical programming deliverables with minimal supervision.Key Responsibilities:- Develop and implement analysis ready datasets, tables, listings, and figures...
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High Performance Computing Systems Expert
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SIRO Clinpharm Pvt. Ltd. | Statistician | india
1 month ago
india SIRO Clinpharm Pvt. Ltd. Full timeStrong general knowledge of statistics and quantitative methods with at least 3 years working in clinical development in the pharmaceutical industry.Knowledge of clinical trial study design, application of appropriate statistical methods, and implementation of simulations (R and SAS).Statistical programming may be required for oversight of deliverables from...
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SIRO Clinpharm Pvt. Ltd. | Statistician | india
1 month ago
india SIRO Clinpharm Pvt. Ltd. Full timeStrong general knowledge of statistics and quantitative methods with at least 3 years working in clinical development in the pharmaceutical industry. Knowledge of clinical trial study design, application of appropriate statistical methods, and implementation of simulations (R and SAS). Statistical programming may be required for oversight of deliverables...