EDC Developer, Programmer

🔥 12 hours ago

🇺🇸 United States – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🖥 Software Engineer

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Celerion

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1971

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

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

• Serve as a subject matter expert in Veeva Clinical Data Management Suite (CDMS), including Veeva Electronic Data Capture (EDC) and Veeva Clinical Database (CDB) • Perform all activities related to eCRF design and EDC build programming for assigned projects • Perform EDC edit check programming for assigned projects based on edit check specifications for both simple and complex edit checks • Create test data to verify both screen design and edit check programming prior to deploying to User Acceptance Testing (UAT) • Set up test environments and coordinate project team members for execution of test scripts • Program and configure listings and reports using clinical reporting tools such as Veeva Clinical Database (CDB) • Ensure secure and high-integrity database imports from vendor transfers using Celerion data transfer standards • Assist with the validation of upgrades to hardware/ software including validation documentation development, review and execution. • 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 EDC systems (i.e. Veeva CDMS, Medidata RAVE, etc.) • Experience with Veeva EDC and Veeva CDB preferred • Proficient computer skills with understanding of clinical systems and data administration • Must be organized, an effective written and oral communicator • Must have the ability to multi-task, within a fast-paced environment, and build strong relationships

🏖️ Benefits

• Celerion Values: Integrity, Trust, Teamwork, Respect • Equal Opportunity Employer