5 дней назад
Senior/Principal Statistical Programmer/Analyst Consultant (Cardiovascular, Renal) (SAS)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior/Principal Statistical Programmer/Analyst Consultant (Cardiovascular, Renal) (SAS): Developing, validating, and maintaining SAS programs, clinical datasets, tables, listings, and figures for cardiovascular, renal, metabolism, respiratory, and immunology studies with an accent on CDISC-compliant SDTM and ADaM data and TLF production. Focus on supporting clinical trial reporting, collaborating with biostatistics and clinical teams, and delivering high-quality programming for regulatory submissions.
Location: Remote, United Kingdom
Company
is a global full-service contract research organization providing clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.
What you will do
- Develop, validate, and maintain SAS programs for clinical study data analysis and reporting.
- Create SDTM and ADaM datasets, tables, listings, and figures according to study requirements.
- Collaborate with Biostatistics, Data Management, Clinical, and client teams.
- Review specifications, participate in study planning, and support regulatory submission activities.
- Ensure programming deliverables meet quality standards and project timelines.
Requirements
- Senior or principal-level experience in clinical statistical programming, including 5 years with a bachelor's degree or 6 years with a master's degree.
- Strong SAS programming experience in the pharmaceutical or CRO industry.
- Hands-on experience supporting cardiovascular, renal, and metabolism studies, plus respiratory or immunology therapeutic-area experience.
- Experience generating and validating SDTM, ADaM, and TLFs, with a good understanding of CDISC standards.
- Working knowledge of ICH, Good Clinical Practices, clinical research, clinical trial processes, and regulatory terminology.
- Ability to work independently, manage multiple priorities, and communicate effectively with stakeholders.
Nice to have
- Experience supporting regulatory submissions.
Culture & Benefits
- Remote consultant engagement outside IR35.
- Opportunity to work directly with a single sponsor while receiving the support and career opportunities of a global CRO.
- Professional development supported through continuous training.
- Work within a quality-focused and supportive environment.
Hiring process
- CV submission followed by an acknowledgement of receipt.
- Phone interview as the first step for candidates meeting the requirements.
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