Clinical Programmer

Job Description

Activities may include, but are not limited to:

·       Build, integrate, and maintain clinical databases and study systems, including transformations, edit checks, reporting, and user testing, while supporting governance of cross‑study programming environments.

·       Design, develop, test, and maintain clinical technology systems (EDC, RTSM, eCOA/ePRO) using programming and automation frameworks.

·       Implement and validate complex data logic such as edit checks, derivations, and dynamic rules.

·       Propose and develop tools to streamline design, build, and validation workflows.

·       Apply data literacy to convert collected data into actionable insights.

·       Develop advanced reporting solutions, including dashboards and visual analytics, using enterprise platforms.

·       Configure, test, and validate data sources for integrations and transformations across systems.

·       Collaborate with stakeholders to translate business needs into technical and system requirements.

·       Troubleshoot routine data ingestion and consumption issues, escalating non‑standard problems appropriately.

·       Develop robust data models, semantic layers, and curated datasets while monitoring pipelines and enforcing quality checks.

·       Validate system functionality and ensure adherence to SOPs, regulations, and compliance standards.

·       Identify process gaps and contribute to continuous improvement initiatives.

·       Maintain audit‑ready documentation for changes, incidents, and system updates.

·       Mentor junior colleagues and contribute to onboarding and knowledge sharing.

·       Support release management activities, including change control and risk assessment.

·       Lead UAT activities, translate requirements into technical specifications, and refine reporting standards.

·       Communicate data and technical findings clearly and partner across teams to enable coordinated, high‑quality delivery.

·       B.A. or B.S. degree, preferably in Biotechnology (primary focus). Candidates from Computer Science, healthcare‑related disciplines, or those with relevant skills and experience may also be considered.

·       Minimum of 3 years experience working in in clinical data programming, data engineering, or related data-management/clinical operations functions.

·       Proficiency in multiple programming languages (SQL, Python, SAS, R) for implementing data collectors, integrations, transformations, and reporting.

·       Skilled with key data‑management tools and platforms, with the ability to adopt new technologies with guidance.

·       Able to execute technical tasks independently on straightforward work, seeking moderate guidance for non‑standard activities.

·       Experienced in scripting and automating data ingestion, cleaning, and reporting processes.

·       Strong understanding of clinical data flow across the study lifecycle (collection, processing, review, reconciliation, reporting).

·       Familiarity with clinical and regulatory data standards, clinical operations, and typical clinical trial data structures.

·       Knowledge of SDLC and validation practices, including change control, release checklists, and traceability.

·       Understanding of GCP, data integrity, audit‑ready documentation, and UAT/sign‑off procedures.

·       Experience optimizing reporting performance and applying data quality controls.

·       Ability to link business needs to technical deliverables using standard procedures.

·       English proficiency of at least B2+ level.

·       Prioritizes tasks, meets deadlines, and maintains clear, organized documentation.

·       Communicates effectively with technical and business partners, adapting style to the audience.

·       Works independently with minimal guidance, using data to triage issues and proactively flag risks with recommended options.

·       Collaborates well across functions, facilitates small working sessions, and follows through on action items.

·       Builds strong cross‑functional relationships and remains open to feedback.

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