Excelra

About the Company

Discover how Excelra, a leader in biopharma data and analytics, uniquely blends scientific understanding with technological expertise. This dual mastery empowers innovative drug discovery and development, transforming research data into actionable insights for groundbreaking discovery.



Excelra's interdisciplinary approach combines life science expertise with cutting-edge technology. This leads to confident, data-centric decisions, simplifying your data-driven drug discovery journey and accelerating your research.



At Excelra, collaboration is key. By co-creating solutions, we amplify your team's capabilities, blending scientific insight and technological acumen for more valuable discoveries and greater project control.

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We navigate the complexities of drug discovery, enhancing your success by structuring chaotic data into actionable insights, leveraging our scientific and technological prowess.



Your goals of faster drug development and better patient outcomes are central to our mission. Committed to delivering insights and tangible progress, we ensure each data point contributes to your innovation journey, helping you 'Excelrate' towards success.



Join us in redefining drug development. Our services span across the life science value chain, from molecule to market. At Excelra, each data point is a step towards a healthier future. Discover how partnering with us can 'Excelrate' your healthcare innovations.

Listed Jobs

Company Name

Excelra

Job Title

eCOA Build Programmer

Job Description

**Job Title:** eCOA Build Programmer **Role Summary** Design, develop, and maintain electronic Clinical Outcome Assessment (eCOA) and electronic Data Capture (eDC) systems. Create validated CRF screens, integrate clinical data workflows, and coordinate with multidisciplinary study teams to support data acquisition, validation, and analytics for clinical trials. **Expectations** - Deliver robust eCOA/eDC build solutions that meet regulatory and protocol specifications. - Manage project deliverables, vendor relationships, and post‑production changes. - Communicate effectively with Data Science, Statistics, PK, Operations, and Medical teams. - Demonstrate problem‑solving, detail orientation, and leadership in fast‑paced environments. **Key Responsibilities** - Design and implement electronic CRF screens with required validations. - Interpret Clinical Protocols and translate terminologies into system specifications. - Analyze study design impact and implement post‑production changes. - Develop data analytics and visualizations for clinical data. - Map data flow from patient to analysis, and select appropriate technology platforms. - Liaise with cross‑functional teams and manage vendor activities. - Apply data standards and medical terminology consistently. - Prioritize multiple tasks, manage ambiguity, and ensure timely delivery. **Required Skills** - Hands‑on programming in eCOA/eDC or Direct Data Capture. - Proficiency in HTML, CSS, JavaScript, Node.js, JSON. - Experience with relational & non‑relational databases (SQL, MongoDB). - Knowledge of data mapping, database structures, and GITLAB utilities. - Understanding of medical terminology and clinical data standards. - Strong analytical, problem‑solving, and attention‑to‑detail abilities. - Excellent written and oral communication; ability to lead and collaborate. **Required Education & Certifications** - Bachelor’s degree in Computer Science, Information Systems, or related field (or equivalent experience). - Relevant certifications in clinical data management or software development (e.g., CDISC, SCRUM) preferred.

United states

Remote

18-03-2026