SysMind, LLC Apply Now Senior eCOA Build Programmer Indianapolis, IN, US

• Posted 5 hours ago

• Updated 5 hours ago Contract W2 Contract Corp To Corp 6 Months No Travel Required On-site $48 - $52/hr Fitment Dice Job Match Score™ To see how well you match this job, please log in or create an account . Once logged in, be sure to complete your profile to get the most accurate match score. Job Details Skills eCOA / Electronic Clinical Outcome Assessment SQL / Database Programming Clinical Data Validation & Testing eCOA / Electronic Clinical Outcome Assessment SQL /

Database Programming Clinical Data Validation & Testing Summary Duration:

6

Months Experience:

8-10

Years Work Location:

Indianapolis , In Job Overview We are seeking an experienced eCOA Build Programmer to design, configure, program, and test electronic Clinical Outcomes Assessment systems used in global clinical trials. The role will focus on clinical data collection, system configuration, data mapping, validation, testing, and integration with clinical data platforms. The ideal candidate will have hands-on experience with eCOA, eDC, eSource, or Direct Data Capture implementations and strong knowledge of clinical data workflows and database technologies. Primary Skills eCOA / Electronic Clinical Outcome Assessment, Clinical Database Programming, eCOA Study Build & Configuration, Clinical Data Management, Clinical Data Mapping Clinical Data Validation & Testing Clinical Trial Systems SQL / Database Programming

HTML / CSS

/ JavaScript Secondary Skills eDC / Electronic Data Capture, eSource / Direct Data Capture, Node.js, JSON, SpEL MongoDB GitLab Data Warehousing Data Analytics & Visualization

EDC / IRT / CTMS

Integrations Data Mapping Clinical Data Standards System Integration Testing UAT / Regression Testing GxP / Validation Clinical Protocol Interpretation Key Responsibilities Review clinical protocols, eCOA requirements, instrument specifications, translations, visit schedules, and edit-check requirements to determine study build scope. Configure and program eCOA studies, including questionnaires, diaries, assessments, visit workflows, notifications, user roles, devices, and data-transfer settings. Translate approved clinical and business requirements into accurate system configurations. Maintain end-to-end traceability between requirements, configuration, testing, and deployment. Develop and maintain build specifications, configuration documentation, test scripts, validation evidence, release notes, and deployment records. Conduct unit testing and support integration, UAT, regression, and production validation activities. Manage defects and change requests, perform impact assessments, and troubleshoot configuration and data issues. Work with instrument owners and licensing teams to ensure approved content, scoring rules, copyright requirements, and language versions are implemented correctly. Coordinate study-build activities across distributed teams and track milestones, dependencies, risks, and issues. Support data integrations between eCOA platforms and clinical systems such as EDC, IRT, CTMS, data warehouses, and analytics environments. Ensure study builds comply with SOPs, documentation practices, validation requirements, data privacy expectations, and applicable regulations. Support production deployment, study go-live, post-production verification, maintenance releases, amendments, and study closeout. Contribute to reusable templates, standards, automation, peer reviews, and continuous improvement of eCOA build processes. Required Qualifications 8-10 years of relevant clinical data / database programming experience. Hands-on experience with eCOA, eDC, eSource, or Direct Data Capture implementations. Experience designing electronic CRF or clinical data collection screens and implementing validations. Strong understanding of clinical protocols and clinical terminology. Experience with clinical data collection tools, workflows, testing, and validation. Strong knowledge of data structures, mapping, normalization, and data flows. Experience with relational and non-relational databases. Strong SQL and database programming experience. Programming experience with HTML, CSS, JavaScript, Node.js, JSON, and/or SpEL. Experience using GitLab or similar source-control tools. Strong analytical, troubleshooting, communication, and collaboration skills. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, and gender identity), national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local law. We are committed to providing reasonable accommodations to qualified applicants with disabilities and for sincerely held religious beliefs, as required by applicable law. Applicants who require a reasonable accommodation during the hiring process may request assistance. Employment may be contingent upon the successful completion of job-related pre-employment screening, which may include background and reference checks and, where permitted by applicable law and applicable to the position, drug testing. All such screening will be conducted in accordance with applicable federal, state, and local laws. Employers have access to artificial intelligence language tools ("AI") that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id:

10114932

Position Id:

139097-9119-1791490662 Posted 5 hours ago Create job alert Never miss an opportunity! Create an alert based on the job you applied for. Create alert Similar Jobs Sierra Business Solution LLC eCOA Build Programmer Indianapolis - IN - Indiana Indianapolis, Indiana

• Today Please strictly adhere to the following resume naming convention: eCOA Build Programmer The electronic Clinical Outcomes Assessment (eCOA) Build Programmer 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. This requires an in depth understanding of data technology, data flow, data standards, database programming, normalization and testing. This role will collabor Third Party, Contract $55 - $60 Eli Lilly and Company Campus - Clinical Data Management Intern Indianapolis, Indiana

• Today At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but i Full-time

USD 76,000.00 - 85,000.00

per year Eli Lilly and Company AI Data Engineering Intern (BS) Indianapolis, Indiana

• Today At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but i Full-time

USD 65,600.00

per year Katalyst Healthcares and Lifesciences Senior RAVE Clinical Database Programmer Remote or New Jersey

•

Today Job Description:

The Senior RAVE Clinical Database Programmer participates in the design, development, validation, and maintenance of clinical study databases. This individual applies advanced knowledge of CRF design, database configuration, edit check programming, custom programming, reporting, system integrations, and CDMS functionality while partnering closely with Clinical Data Management and cross-functional study teams to support successful clinical trial execution.

Key Responsibilities:

Full-time Search all similar jobs More jobs at SysMind, LLC in Indianapolis, IN