Clinical Database Manager

Summary

Join Precision for Medicine as a Senior/Principal Clinical Database Manager and contribute to the design, development, testing, implementation, maintenance, and support of clinical databases and applications. Work remotely from the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia. Collaborate with internal teams, vendors, and clients to gather requirements and provide updates. Train end-users and junior staff. Lead internal software projects involving specialized programming and scripting. Apply your expertise in clinical data management, database systems, and programming languages to advance oncology research and development. Precision Medicine Group is an Equal Opportunity Employer.

Requirements

• Have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline
• Have a Bachelor’s degree or a combination of related experience
• Have Rave API integration experience using external vendor modules
• Have Rave Advanced Custom Function programming experience
• Be proficient in Microsoft Office: Word, Excel, PowerPoint, Outlook
• Be able to handle a variety of clinical research tasks
• Possess excellent organizational and communication skills
• Be able to professionally use the English language, both written and oral
• Have experience in Object Oriented Programming (C#, C++, VBS, etc.), scripting language (PERL, etc.), SAS, R, SQL
• Have an understanding of CDISC standards (CDASH, SDTM, ADaM, etc.)
• Have experience in clinical database management system development
• Have experience in a clinical, scientific or healthcare discipline
• Have experience in utilizing various clinical database management systems
• Have broad knowledge of drug, device and/or biologic development and effective data management practices
• Possess strong leadership and interpersonal skills
• Be able to communicate effectively in the English language

Responsibilities

• Design clinical databases and applications
• Develop clinical databases and applications
• Test clinical databases and applications
• Implement clinical databases and applications
• Maintain clinical databases and applications
• Support clinical databases and applications
• Interface with internal team (Data Management, Project Management, etc.)
• Interface with EDC vendor
• Interface with clients
• Interface with third-party vendors
• Gather requirements from stakeholders
• Provide status updates to stakeholders
• Provide operational and technical training to end users
• Provide operational and technical training to junior staff
• Play a lead role in internal software projects
• Perform specialized programming for internal software projects
• Perform scripting for internal software projects

Preferred Qualifications

• Have oncology and/or Orphan Drug therapeutic experience
• Have experience with Base SAS®, SAS/STAT and SAS/ACCESS software
• Have experience with SAS Macro programming language
• Have advanced experience in Database Management and object-oriented programming
• Have Veeva set up experience