Katalyst CRO, located in Cambridge, Massachusetts, is looking for a Clinical Database Designer. The role involves designing and configuring clinical study databases within EDC/CDM platforms while ensuring adherence to client needs and compliance standards. Responsibilities include leading study builds, configuring workflows, mentoring team members, and managing project deliverables. Candidates should have extensive knowledge of clinical trial processes and experience with Medidata Rave, Oracle Clinical, and OpenClinica. Excellent communication and analytical skills are crucial for success in this role.
Qualifications
Strong knowledge of Clinical Trial Processes.
Hands-on experience with Medidata Rave, Oracle Clinical, and OpenClinica.
Expertise in study database build and configuration.
Understanding of CDISC/Data Standards/Data Management.
Experience with UAT, QC Testing, and Functional Documentation.
Knowledge of Integrations/Data Migration.
Strong analytical and problem-solving skills.
Excellent communication and stakeholder management skills.
Experience in team leadership and mentoring.
Responsibilities
Lead Study Build and Database Configuration in EDC systems.
Configure Edit Checks, Workflows, and Validations.
Gather and translate client requirements into solutions.
Create Specifications, Test Cases, and provide UAT Support.
Support integrations and data transfers with vendors.
Deliver client workshops (remote/on-site).
Manage timelines, budgets, and project deliverables.
Resolve implementation and configuration issues.
Provide status reports to stakeholders.
Mentor junior team members and train new hires.
Drive process improvements and best practices.
Ensure SOP and compliance adherence.
Skills
Clinical Trial Processes
Medidata Rave
Oracle Clinical
OpenClinica
Analytical skills
Problem-solving skills
Communication skills
Stakeholder management
Team leadership
Job description
Katalyst CRO, located in Cambridge, Massachusetts, is looking for a Clinical Database Designer. The role involves designing and configuring clinical study databases within EDC/CDM platforms while ensuring adherence to client needs and compliance standards. Responsibilities include leading study builds, configuring workflows, mentoring team members, and managing project deliverables. Candidates should have extensive knowledge of clinical trial processes and experience with Medidata Rave, Oracle Clinical, and OpenClinica. Excellent communication and analytical skills are crucial for success in this role.