Senior Clinical Database Programmer

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    Skills

    • Acceptance Testingunmatched
    • Analysis Skillsunmatched
    • Best Practicesunmatched
    • Budget Managementunmatched
    • Clinical Dataunmatched
    • Clinical Data Interchange Standards Consortium (CDISC)unmatched
    • Clinical Data Managementunmatched
    • Clinical Trialunmatched
    • Communication Skillsunmatched
    • Configuration Managementunmatched
    • Customer/Client Researchunmatched
    • Data Collectionunmatched
    • Data Managementunmatched
    • Data Migrationunmatched
    • Database Administrationunmatched
    • Database Programmingunmatched
    • Documentationunmatched
    • Electronic Data Capture (EDC)unmatched
    • Functional Testingunmatched
    • Maintain Complianceunmatched
    • Mentoringunmatched
    • Oracleunmatched
    • Problem Solving Skillsunmatched
    • Procedure Implementationunmatched
    • Process Improvementunmatched
    • Quality Controlunmatched
    • Reporting Skillsunmatched
    • Requirements Managementunmatched
    • Status Reportsunmatched
    • Systems Administration/Managementunmatched
    • Team Lead/Managerunmatched
    • Test Caseunmatched
    • Time Managementunmatched

    Description

    Job Description:
    Design, build, and configure clinical study databases in EDC/CDM platforms. Ensure systems meet client needs, follow GCDMP, support accurate data capture, workflows, edit checks, and integrations.
    Responsibilities:
    • Lead Study Build / Database Configuration in EDC systems.
    • Configure Edit Checks, Workflows, Validations.
    • Gather & translate client requirements into solutions.
    • Create Specifications / Test Cases / UAT Support.
    • Support integrations & data transfers with vendors.
    • Deliver client workshops (remote/on-site).
    • Manage timelines, budgets & project deliverables.
    • Resolve implementation / configuration issues.
    • Provide status reports to stakeholders.
    • Mentor junior team members / train new hires.
    • Drive process improvements & best practices.
    • Ensure SOP / compliance adherence.
    Requirements:
    • Strong knowledge of Clinical Trial Processes.
    • Hands-on experience with Medidata Rave, Oracle Clinical, OpenClinica.
    • Study database build & configuration expertise.
    • Understanding of CDISC / Data Standards / Data Management.
    • UAT, QC Testing, Functional Documentation.
    • Integrations / Data Migration knowledge.
    • Strong analytical & problem-solving skills.
    • Excellent communication & stakeholder management.
    • Team leadership / mentoring experience.

    Numbers & Facts

    LocationEdison, NJ

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