The Senior Statistical Programmer Consultant leads and/or supports programming efforts to deliver
Delivery-focused role requiring high technical skills and industry knowledge to independently
Collaborates with Biostatistics, Data Management, and Clinical teams to meet study requirements and

🎯 Requirements

Strong SAS programming experience within the pharmaceutical/CRO industry
Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies
Experience generating and validating SDTM, ADaM, and TLFs
Good understanding of CDISC standards and clinical trial processes
Ability to work independently and manage multiple priorities in a fast-paced environment
Experience supporting regulatory submissions is preferred

🎁 Benefits

Client-facing role with global CRO opportunities
Security and career development in a global environment

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