Senior Clinical Database Programmer
Katalyst CRO
Role Summary 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. Role Summary 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. Key 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 Required Skills: 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 #J-18808-Ljbffr
Vacancy posted 3 days ago
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