CRO Solutions® is looking for a Statistical Programmer to work within our growing multidisciplinary Biometrics team. The role can either be remote-based with occasional visits to our Salford Quays office or office-based.
Responsibilities
* Statistical Programming Support: Develop, test, and validate SAS® programs for datasets, tables, listings, and figures under the guidance of a Lead Programmer.
* CDISC Implementation: Assist in mapping and applying CDISC standards to datasets and documentation.
* Study Delivery: Contribute to the delivery of statistical programming deliverables across various phases of clinical studies.
* Collaboration: Work closely with Statisticians, Data Managers, and other Programmers as part of cross‑functional study teams.
* Quality Focus: Follow internal quality processes and ensure outputs meet industry and regulatory standards.
* Career Development: Grow your programming skills and gain exposure to new tools and processes as part of a supportive team.
* Additional context: CRO Solutions® are reinventing the way we perform statistical analysis, how we track our studies, how we define our internal standards and how we create our datasets and outputs. The candidate must have strong SAS® programming skills, with at least 2 years of hands‑on experience in clinical trials. Familiarity with CDISC standards (SDTM and/or ADaM) is required; training and support will be provided. A degree in Mathematics, Computer Science, Life Sciences, or a related field is advantageous, though equivalent experience is welcome. A collaborative mindset, attention to detail, and a willingness to learn and grow. Experience with Phase I / Early Phase studies or R programming is a plus but not required.
Qualifications
* SAS® Expertise: Strong knowledge of SAS® programming for data analysis and reporting.
* CDISC Standards: Working knowledge of CDISC standards (SDTM, ADaM) and their implementation.
* Educational Background: Degree in Mathematics, Computer Science, or a related field, or equivalent professional experience.
* Internal Standards Development: Ability to use internal programming standards and processes.
* Project Support: Experience in supporting the Lead Programmer with the programming aspects of clinical studies.
* Collaboration: Strong ability to liaise with the other Programmers to promote department collaboration.
Desirable Skills
* Early Phase Trials: Experience with Phase I / Early Phase clinical trials.
* Macro Development: Experience in developing standard macros to improve efficiency.
* Self-Starter: Willingness to jump in headfirst to show initiative and continue to drive innovation.
* Cross‑Functional Development: Involvement in department process development initiatives, e.g., standards development.
Benefits
* Immediate Start: Get started right away and begin making an impact.
* Career Progression: Numerous opportunities for advancement within the company.
* Professional Development: Continuous learning and development to enhance your skills and career.
* Generous Annual Leave: 29 days of annual leave plus Bank Holidays, increasing to 33 days after 5 years of service.
* Pension Scheme: Company pension plan to secure your future.
* Annual Bonus: Annual bonus based on company performance.
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