Principal Database Programmer

🔥 0 minutes ago

🇷🇸 Serbia – Remote

⏰ Full Time

🔴 Lead

🖥 Software Engineer

👻 Ghost score 23%

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Logo of Precision Medicine Group

Precision Medicine Group

1001 - 5000 employees

Founded 2012

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 $35.2M Venture Round on 2021-03

Consulting • Healthcare • Logistics

Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.

📋 Description

• Manage all programming aspects of clinical databases and applications from study start through post database lock • Ensure on-time delivery and communicate project status to internal teams and study teams • Monitor contract elements and scope of work for assigned projects • Forecast project hours, identify resource requirements, and manage project budgets • Provide input and guidance on clinical database design • Build and support clinical databases • Develop, test, and validate programs and clinical databases for client projects and third-party applications • Provide system administration and advanced technical support • Troubleshoot and resolve software and clinical database problems • Develop and maintain study-specific validation documents • Support data management from CRF design through database close and archival • Participate in software vendor selection, EDC demonstrations, trainings, and SOP development • Support onboarding of new hires and lead cross-functional initiatives • Train data management project team members • Communicate with sponsors, vendors, and project teams regarding project issues • Present software demonstrations, trainings, and project meetings • Perform duties in accordance with SOPs, government regulations, guidelines, and industry standards • May require some travel and other duties as assigned

🎯 Requirements

• Minimum 8 years’ experience • Bachelors and/or a combination of related experience • Strong experience in Oncology; experience with Autoimmune diseases would be a strong advantage • Strong experience with Rave and Veeva • Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook • Experience in Object Oriented Programming (C#, C++, VBS, etc.) • Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.) • Proficiency in more than one CDMS system, including building forms, edit checks and complex rule development • Awareness of CRF standards and input to maintenance of standards library • Ability to troubleshoot and support peers with technical issues and build solutions • Broad knowledge of drug, device and/or biologic development and effective data management practices • Able to handle a variety of clinical research tasks • Excellent organizational and communication skills • Professional use of the English language, both written and oral • Experience in clinical database management system development • Experience in a clinical, scientific or healthcare discipline • Strong leadership and interpersonal skills

🏖️ Benefits

• Full-time, permanent position • Fully remote work from European locations • Equal opportunity employment • Reasonable accommodation available for applicants with disabilities

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