Senior/Principal Clinical Database Manager

Summary

Join Precision for Medicine as a Senior/Principal Clinical Database Manager! This remote position (UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia) involves designing, developing, testing, implementing, maintaining, and supporting clinical databases and applications. You will collaborate with internal and external teams, providing training and potentially leading internal software projects. The role requires extensive experience in clinical database management, specific software proficiency, and strong communication skills. Oncology and/or Orphan Drug therapeutic experience is preferred. Precision for Medicine offers a unique opportunity to contribute to advancements in cancer treatment.

Requirements

• Have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline
• Possess a Bachelor’s degree and/or a combination of related experience
• Be Medidata Rave EDC Certified Study Builder
• 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.), EDC vendor, clients, and third-party vendors
• Gather requirements and provide status updates
• Provide operational and technical training to end users and junior staff
• Play a lead role in internal software projects requiring specialized programming and/or scripting

Preferred Qualifications

• Have Oncology and/or Orphan Drug therapeutic experience
• Be proficient in 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