Job Description

Our client is looking for a Lead Programmer to join their team - this role is remote.

Responsibilities:

• Provide technical support and expert advice to internal staff and external sponsors.
• Lead projects for SAS programming activities including assigning programming tasks to different team members, monitoring quality, timelines, resource allocation, and productivity in relation to budgets. 
• Provide oversight and guidance on complex trials and submission projects (including Integrated Summary of Safety or Efficacy). 
• Assist in the review of statistical analysis plans and TLF shells; create and/or review the ADaM and SDTM dataset specifications, CRF annotation, and other process supporting documents.
• Produce and/or QC derived datasets, tables, figures and data listings. 
• Understand regulatory requirements concerning industry technical standards (e.g., CDISC, electronic submissions, etc.) and implications for the department. 
• Create SAS  macros and template programs s to improve the efficiency of SAS programming activities.
• Mentor statistical programmers.

Qualifications:

• Proficiency in SAS
• Bachelor’s degree and 5 years relevant CDISC and clinical trial industry experience or equivalent combination of training and experience
• Project leadership experience
• Advanced proficiency level in English – spoken and written