
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.
🔥 0 minutes ago
Improve your chances of getting an interview by checking your resume score before you apply.

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.
• Manage all programming aspects of clinical databases and applications from study start through post database lock • Lead operational study teams and programming team members on assigned studies and study programs • Provide operational and technical training to end users, junior staff, and data management project team members • Provide planning estimates for project scope, schedules, forecasting, and resource requirements • Maintain assigned projects and ensure on-time delivery • Communicate project status and contract/scope updates to internal teams and study teams • Forecast project hours, identify resource requirements, and manage project budgets, out-of-scope work, and post-production changes • Provide input and guidance on clinical database design to clients and internal teams • Build, support, develop, test, and validate clinical databases, programs, 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, SOP development, and process documentation • Support onboarding of new hires • Provide leadership for cross-functional and organization-wide initiatives • Communicate with study sponsors, vendors, and project teams regarding project issues • Present software demonstrations, training sessions, and project meetings • Perform duties in accordance with SOPs, government regulations, guidelines, and industry standards • May require some travel • Perform other duties as assigned
• Minimum 8 years’ experience • Bachelors and/or a combination of related experience • Strong experience in Oncology • Experience with Autoimmune diseases would be a strong adventage • 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
• Full-time, permanent position • Fully remote work from European locations • Equal Opportunity Employer • Reasonable accommodation available for the application process
Apply Now