Senior/Principal Clinical Database Manager

Summary

Join Precision for Medicine as a Senior/Principal Clinical Database Manager and work remotely from the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia. You will be responsible for designing, developing, testing, implementing, maintaining, and supporting clinical databases and applications. This role involves interfacing with internal teams, vendors, and clients, providing training, and potentially leading internal software projects. The position requires experience in clinical data management databases, Rave API and Advanced Custom Function programming, proficiency in Microsoft Office and various programming languages, and a strong understanding of CDISC standards. Excellent communication and organizational skills are essential. Preferred qualifications include oncology/orphan drug experience and expertise in specific software and programming languages.

Requirements

• Have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline
• Have a Bachelor’s degree and/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
• Have professional use of 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
• Provide status updates
• Provide operational and technical training to end users and junior staff
• Play a lead role in internal software projects that require specialized programming and/or scripting

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, object-oriented programming
• Have Veeva set up experience