eCOA Build Programmer – Technical Analyst in Bangalore

Job Description

Join American pharmaceutical leader Eli Lilly and Company, currently hiring eCOA Build Programmer – Technical Analyst in Bangalore, Apply Lilly careers in Bangalore Karnataka.

 

Position : eCOA Build Programmer – Technical Analyst

Location : Bengaluru, India

Job id: R-32616

 

Job Details

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.eCOA Build Programmer – Technical AnalystJob DescriptionAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 39,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the worldThe electronic Clinical Outcomes Assessment (eCOA) Build Programmer – IT Analyst is responsible for designing, programming and testing clinical trial data collection databases, including the mapping, testing and normalization of data into a clinical data warehouse. In addition, this role will serve as a technical expert to the eCOA SaaS Platform and working on the customizations needed for the Clinical Data Collection and reporting. This role will collaborate with Data and Analytics colleagues such as the Clinical Data Associate, Clinical Data Manager, Statistician and other key partners to deliver standardized data collection methods and innovative validation solutions for use in global clinical trials.Responsibilities:This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.
 High agility to digest and demonstrate the ability to understand and extend the capabilities of the platform to meet the deliverables.Understands requirements and effectively translates design needs and process into technical terms, and vice versa Participates in design reviews to ensure traceability of requirements. Collobrate with appropriate colleagues to determine solutions to meet design needs. Seeks opportunities to reuse existing processes and services to streamline support and implementation of key systems.  Stay current with the tools and technologies to influence design strategy so that it provides best usage opportunities for the portfolio delivery.Partner with and influence vendor resources on solution development to ensure understanding of data and technical direction for solutions as well as delivery.Adapt quickly in a constantly changing environment.Assist study teams with the customization of screens using HTML, CSS, JAVASCRIPT with the eCOA SaaS platformAssist study teams with data mapping, data integration, reporting and data exportsModify existing systems or integrate packaged systems with existing infrastructure to meet design requirementsCreate Python and Node.JS scripts to enable job controls within the SaaS platformAssist in developing and delivering custom reports for tracking the Study status, compliance and data completion. Produce and maintain project documentation as required, including that of Computer Systems QualityUse standard processes for requirements definition, analysis, design, construct, and test activitiesPortfolio Delivery:Gather and influence eCOA design specifications to enable successful trial implementationProgram and test data collection systems and associated data repository mappings for a trial or set of trials within a program using data standards library componentsEnsure data collection systems and data warehouse mappings are delivered accurately, efficiently and in alignment with study objectivesPartner with Clinical Build Programmer to ensure complete data build for trial data collection needsProvide insights into study level deliverables (i.e., Data Management Plan, Project Plan, database, and observed datasets)Support submission, inspection and regulatory response activitiesLead cross Business Unit/Therapeutic Area projects or programs with high complexityOpportunity to develop and tests new ideas and/or applies innovative solutions that add new value to the portfolioProject Management:Increase speed, accuracy, and consistency in the development of systems solutionsEnable metrics reporting of study development timelines and pre and postproduction changes to databasePartner to deliver study database per business need and before first patient visitFollow and influence data standard decisions and strategies for a study and/or programUtilize therapeutic knowledge and possess a deep understanding of the technology used to collect clinical trial dataApply knowledge of applicable internal, external and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to study build deliverablesIntegrate multi-functional and/or external information and applies technical knowledge to data-driven decision making
Enterprise Leadership:Seek and implement means of improving processes to reduce study build cycle time, decrease work effort and enable the normalization of various sources of data into a common data repository in a way that allows for improved integration, consumption and downstream analysisRepresent Data and Analytics processes in multi-functional initiativesEngage in shared learning across Data and Analytics organizationIncrease re-usability of screens and edits by improving the initial designReduce postproduction changes change control processAnticipate and resolve key technical, operational or business problems that impact the Data and Analytics organizationInteract with regulators, business partners and outside stakeholders on business issuesThink end to end in mind to consistently manage risk and minimize impact on deliveryBuild a diverse multi-functional and internal/external network to understand how different disciplines and approaches contribute to research and developmentFocuse on defining database solutions and timelines in support of advancing the portfolio
 Minimum Requirements:Bachelor’s or Master’s degree in computer science, engineering, medical field, Informatics, Life Sciences, Statistics, Information Technology, with 3 or more years of hands-on experience in database programming, or clinical data management, system validation and data analysis.Technical proficiency with HTML, CSS, JAVASCRIPT, Data Mapping, understanding of database structures, ETL, etc.2 – 8 years of development experience programing with Node.js or Python and JSON.2+ years of experience with relational and non-relational database technologies utilizing SQL, Data Functions and Procedures. (e.g. Oracle,  PostgreSQL, MongoDB,  DynamoDB)Experience with mobile development and calling API’s to obtain or share content with a SaaS PlatformExperience handling GITLAB utilitiesDemonstrated learning agility both technically as well as business processes and applicationsDemonstrated initiative to build relationships, learn new business processes and identify opportunitiesDemonstrated ability to proactively identify issues and either resolve or escalate to the appropriate level for resolutionStrong problem-solving skillsGood communication skills (written/oral)Process improvement skillsOrganization skillsSelf-managementDemonstrated ability to evaluate, facilitate, and drive towards risk-based decision making
 Additional Preferences:Knowledge on Clinical Research and/or applications collecting or managing data for Clinical trialsTechnical proficiency with eCOA (electronic Clinical Outcome Assessment) or eDC (electronic data capture), eSource or Direct Data Capture implementationHas worked with organizations that provide software-as-a-service (SaaS).Data analytics and visualizationsArticulating the flow of data (structure and format) from patient to analysis and apply this knowledge to data solutionsDeciding the technology platform (system/database) for data acquisition and aggregationFamiliarity with clinical data tools and technologiesUnderstanding and experience in using data standardsKnowledge of medical terminologyOther Information:Domestic and International travel may be requiredEli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( Lilly_Recruiting_Compliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

 

 

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