Senior Statistical Programmer (CVRM)

TL;DR

Senior Statistical Programmer (CVRM): Developing and validating clinical study data analysis and reporting components with an accent on CDISC standards and regulatory submissions. Focus on creating SDTM, ADaM, and TLFs for cardiovascular, renal, and metabolism studies while managing stakeholder expectations in a client-facing environment.

Location: Must be based in the United Kingdom

Company

hirify.global is a global full-service CRO providing clinical development and functional solutions for pharmaceutical, biotechnology, and medical device companies.

What you will do

• Develop, validate, and maintain SAS programs for clinical study data analysis and reporting.
• Create datasets, tables, listings, and figures (TLFs) according to study requirements.
• Collaborate with Biostatistics, Data Management, and Clinical teams to ensure high-quality deliverables.
• Lead or support programming efforts under the direction of a team leader.
• Participate in study planning, review specifications, and support regulatory submission activities.

Requirements

• Must be based in the United Kingdom.
• Strong SAS programming experience within the pharmaceutical or CRO industry.
• Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies.
• Experience in generating and validating SDTM, ADaM, and TLFs.
• Good understanding of CDISC standards and clinical trial processes.
• Bachelor’s degree with 5+ years or Master’s degree with 6+ years of clinical programming experience.

Nice to have

• Experience supporting regulatory submissions.
• Respiratory or Immunology therapeutic area experience.

Culture & Benefits

• Supportive, quality-focused global CRO environment.
• Opportunities for professional development and continuous training.
• Client-facing role with the security of a global organization.
• Emphasis on diversity, inclusivity, and employee well-being.

Hiring process

• Initial CV review and acknowledgement.
• Phone interview for qualified candidates.