Design, development, testing, implementation, maintenance and support of clinical databases and applications
Interface with internal teams (Data Management, Project Management), EDC vendor, clients and third-party vendors to gather requirements and provide status updates
Provide operational and technical training to end users and junior staff
Potential lead role in internal software projects requiring specialized programming and/or scripting
Requirements
Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline
Bachelor’s and/or a combination of related experience
Rave API integration experience using external vendor modules
Rave Advanced Custom Function programming experience
Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
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 Object Oriented Programming (C#, C++, VBS, etc.)
Experience with scripting languages (PERL, etc.)
Experience with SAS, R, SQL
Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.)
Experience in clinical database management system development
Experience in a clinical, scientific or healthcare discipline
Experience in utilizing various clinical database management systems
Broad knowledge of drug, device and/or biologic development and effective data management practices
Strong leadership and interpersonal skills
Must be able to communicate effectively in the English language
Preferred: Oncology and/or Orphan Drug therapeutic experience
Preferred: Base SAS®, SAS/STAT and SAS/ACCESS software
Preferred: SAS Macro programming language
Preferred: Advanced experience in Database Management, object-oriented programming