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, clients, and third-party vendors. You will provide training to end-users and junior staff and may lead internal software projects. Precision for Medicine is revolutionizing cancer treatment by using biomarkers to link mutations to treatments and employing advanced technology and expertise in clinical trials. The company delivers robust insights for real-time decisions and optimizes the oncology development pathway.

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
• 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 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, object-oriented programming
• Have Veeva set up experience