Remote Principal SAS Programmer

Summary

Join us as a Principal SAS Programmer to program metrics, reports, and tools for clinical trial data cleaning processes.

Requirements

• 12+ years’ experience
• Bachelor's degree or equivalent in local country or equivalent level of 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 utilizing various clinical database management systems
• Experience in a clinical, scientific or healthcare discipline
• Advanced computer skills • Base SAS®, SAS/STAT and SAS/ACCESS
• SAS Macro Language • Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.…)
• Broad knowledge of drug, device and/or biologic development and effective data management practices
• Strong leadership and interpersonal skills

Responsibilities

• Maintains the full-scope of responsibility for assigned projects: ensures on-time delivery, communicates the status of projects to internal teams and study
• Provides collaborative input and guidance to the design of SAS outputs to the client and internal teams
• Programs metrics, reports, tools, patient profiles
• Develops, tests, and validates SAS programs to support client-related and cross-functional projects
• Troubleshoots and resolves SAS program issues
• Develops and maintains SAS programming validation documents
• May provide biostatistics support for client-related projects which may include tables, listings, figures, SDTM, ADaM and various other CDISC deliverables
• May provide data management support for client-related projects from CRF design to post database close and archival
• Participate in conducting demonstrations and trainings
• Participate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to SAS programming activities
• Provide leadership for cross-functional and organization-wide initiatives, where applicable
• Train project team members
• Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues
• Present software demonstrations/trainings, department/company training sessions, present at project meetings

Preferred Qualifications

• Experience in Object Oriented Programming (C#, C++, VBS, etc.), scripting language (PERL, etc.), R, SQL
• Oncology and/or Orphan Drug therapeutic experience