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Principal Statistical Programmer/Analyst Consultant Remote at UK (CVRM- Cardiovascular , Renal & Metabolism)-(Outside IR35)

6 hours, 36 minutes ago
United Kingdom
Contract
Lead
Data Scientist
Software Development
Apply Now
ClinChoice

ClinChoice

ClinChoice is a leading full-service contract research organization (CRO) that provides high-quality solutions to clients in the pharmaceutical, biotechnology, medical device, and consumer products sectors, focusing on accelerating the development and ...

Professional Services
1K-5K
Founded 1995
View All Jobs 4

Description

  • Develop, validate, and maintain SAS programs for clinical study data analysis and reporting.
  • Create datasets, tables, listings, and figures according to study requirements.
  • Collaborate with Biostatistics, Data Management, and Clinical teams.
  • Ensure programming deliverables meet quality standards and project timelines.
  • Participate in study planning, review specifications, and support submission activities.
  • Lead and/or support programming efforts under the direction of a Programming team leader.
  • Work independently to deliver technical programming and information components of the project.

Requirements

  • Bachelor’s degree in computer science, statistics, or a related scientific discipline with 5 years of clinical programming (CDISC) experience, or a Master’s degree with 6 years of clinical programming (CDISC) experience.
  • Strong SAS programming experience within the pharmaceutical or 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.
  • Strong communication and stakeholder management skills.
  • Experience supporting regulatory submissions is preferred.
  • Need to have Respiratory/Immunology therapeutic area experience.
  • Working knowledge of ICH, Good Clinical Practices, clinical research, clinical trial processes, and related regulatory requirements and terminology.

Benefits

  • Opportunity to work directly for a single sponsor while employed through a global CRO.
  • Remote work designation implied by the listing tags.
  • Professional development and supportive culture.
  • Global CRO environment with additional career opportunities.
  • Equal opportunity employer with a commitment to diversity and inclusivity.

Interested in this position?

Apply directly on the company website

Apply Now

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