Principal Database Programmer

🔥 0 minutes ago

🇷🇸 Serbia – Remote

⏰ Full Time

🔴 Lead

🖥 Software Engineer

👻 Ghost score 10%

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Precision For Medicine

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 $75M Private Equity Round on 2015-12

Healthcare • Consulting • Logistics

Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.

📋 Description

• Manage all programming aspects of clinical databases and applications from study start to post database lock • Maintain responsibility for assigned projects and ensure on-time delivery • Communicate project status, contract scope and work updates to internal teams and study teams • Forecast project hours, identify resource requirements and manage project budgets • Provide input and guidance on clinical database design • Build, support, develop, test and validate clinical databases, programs and 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 and trainings • Contribute to SOP and process documentation development and maintenance • Lead operational study teams and programming team members • Provide operational and technical training to end users, junior staff and data management project team members • Support onboarding of new hires • Provide leadership for cross-functional and organization-wide initiatives • Communicate with sponsors, vendors and project teams regarding project issues • Present software demonstrations, training sessions and project meetings • Perform duties in accordance with SOPs, regulations, guidelines and industry standards • Perform other assigned duties

🎯 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 • Ability to handle a variety of clinical research tasks • 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 • May require some travel