Design, develop, test, implement, maintain and support clinical databases and applications
Interface with internal teams (Data Management, Project Management, etc.), 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
Play a lead role in internal software projects requiring specialized programming and/or scripting
Support Rave API integrations and Advanced Custom Function programming tasks
Apply CDISC standards and effective data management practices in database development
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.…), scripting language (PERL, etc.), 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.
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 (Preferred)