Excelra · 3 weeks ago
eCOA Build Programmer
Excelra is a company focused on clinical data solutions, and they are seeking an eCOA Build Programmer to design electronic CRF screens and implement data capture solutions. The role involves analyzing clinical data workflows, collaborating with study teams, and managing project and vendor relationships.
Responsibilities
Handson experience as programmer in eCOA (electronic Clinical Outcome Assessment) or eDC (electronic data capture), eSource or Direct Data Capture implementation
Design of electronic CRF screens to capture Clinical data and build on required validations
Understanding of Clinical Protocol and interpretation of the Clinical terminologies to create or design specifications
Familiarity with Clinical data tools, technologies, workflow for collecting patient data, testing and validation of system
Analyse the impact and implement post production changes the Study design
Data analytics and visualizations
Articulating the flow of data (structure and format) from patient to analysis and apply this knowledge to data solutions
Deciding the technology platform (system/database) for data acquisition and aggregation
Utilization of clinical/drug development knowledge and an ability to liaise effectively with study team members (i.e., Data Sciences, Statistics, PK, Operations, Medical)
Strong therapeutic/scientific knowledge in the field of research
Project management experience
Vendor management experience
Understanding and experience in using data standards
Knowledge of medical terminology
Ability to balance multiple activities, prioritize and manage ambiguity
Demonstrated exemplary teamwork/interpersonal skills
Proven problem solving, attention to detail and result oriented behaviors in a fast-paced environment
Qualification
Required
Handson experience as programmer in eCOA (electronic Clinical Outcome Assessment) or eDC (electronic data capture), eSource or Direct Data Capture implementation
Design of electronic CRF screens to capture Clinical data and build on required validations
Understanding of Clinical Protocol and interpretation of the Clinical terminologies to create or design specifications
Familiarity with Clinical data tools, technologies, workflow for collecting patient data, testing and validation of system
Analyse the impact and implement post production changes the Study design
Data analytics and visualizations
Articulating the flow of data (structure and format) from patient to analysis and apply this knowledge to data solutions
Deciding the technology platform (system/database) for data acquisition and aggregation
Utilization of clinical/drug development knowledge and an ability to liaise effectively with study team members (i.e., Data Sciences, Statistics, PK, Operations, Medical)
Strong therapeutic/scientific knowledge in the field of research
Project management experience
Vendor management experience
Understanding and experience in using data standards
Knowledge of medical terminology
Ability to balance multiple activities, prioritize and manage ambiguity
Demonstrated exemplary teamwork/interpersonal skills
Proven problem solving, attention to detail and result oriented behaviors in a fast-paced environment
Preferred
Programming experience with HTML, CSS, JAVASCRIPT, Node.js, JSON
Experience with relational and non-relational database technologies utilizing SQL, Data Functions and Procedures. (e.g., MongoDB)
Technical proficiency with HTML, Data Mapping, understanding of database structures, etc
Experience handling GITLAB utilities
Quick learner to new trends in technology
Excellent leadership, communication (written and oral) and interpersonal skills
Demonstrated leadership in professional setting
Company
Excelra
Excelra is a leading Informatics company providing Intelligent data and analytics solutions to clients globally.
Funding
Current Stage
Late StageTotal Funding
$0.65M2016-06-29Seed· $0.65M
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