Clinical Database Programmer

🔥 7 minutes ago

🇺🇸 United States – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🖥 Software Engineer

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Celerion

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1971

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Celerion is a global leader in clinical research services with a focus on accelerating drug development through translational medicine. The company offers a range of services including early phase clinical trials, bioanalytical sciences, PK/PD studies, biomarkers, and regulatory affairs. Celerion is dedicated to getting drugs to market faster by leveraging their experience and innovative research strategies. Their expertise covers various therapeutic areas such as oncology, metabolic and respiratory diseases, biosimilars, and vaccines. With over 40 years of experience, Celerion has been recognized for their leadership in the clinical research organization (CRO) space and is committed to science and technology-driven innovations that advance healthcare solutions globally.

📋 Description

• Administer EDC databases for client-contracted clinical trial projects • Evaluate protocols and requirements • Design and build electronic case report forms (eCRFs) with corresponding edits • Troubleshoot and escalate system problems to appropriate partners • Interact technically with application-supporting vendors • Provide expert guidance on study set-up design, development, validation, implementation, and maintenance • Manage EDC trial deployment • Set up interface connections between EDC and other systems • Perform eCRF design and EDC build programming • Program simple and complex EDC edit checks • Create test data to verify screen design and edit-check programming before UAT • Set up test environments and coordinate project team members executing test scripts • Configure listings and reports using Veeva Clinical Database and clinical reporting tools • Ensure secure, high-integrity database imports from vendor transfers using Celerion data transfer standards • Assist with hardware/software upgrade validation and related documentation • Maintain global clinical trial database standards (CDISC)

🎯 Requirements

• Bachelor’s degree in a related field preferred • 3 years of clinical data management experience • Ability to program using SQL required • Experience with Veeva EDC and Veeva CDB • Proficient computer skills and understanding of clinical systems and data administration • Organized, effective written and oral communicator • Ability to multitask in a fast-paced environment and build strong relationships

🏖️ Benefits

• Travel for training and key meetings