ICON plc este o organizație globală de cercetare în regim contractual, care deservește industriile din domeniul sănătății și farmaceutic. Activitatea sa cuprinde servicii clinice, de consultanță și comerciale care sprijină dezvoltarea medicamentelor, de la cercetarea timpurie până la activitățile post-comercializare. Compania oferă soluții precum studii clinice descentralizate, evaluarea siguranței cardiace, laboratoare clinice pentru etapele timpurii, imagistică medicală, informații de reglementare și dovezi din lumea reală. ICON plc dispune, de asemenea, de expertiză terapeutică în domenii precum bolile cardiovasculare, oncologia, medicina internă, terapiile celulare și genice și medicamentele biosimilare, combinând analiza datelor cu o abordare axată pe pacienți pentru a contribui la avansarea programelor clinice.
Statistical Programmer, Clinical Trials — ICON plc (Tokyo Hybrid)
Develop and validate SAS, R, and Python programs supporting clinical-trial data analysis and reporting at ICON plc. Partner with biostatistics and clinical teams on regulatory documentation and treatment-development activities.
Descriere
- Create, validate, and maintain SAS, R, or comparable statistical programs for clinical-trial data processing, analysis, and reporting
- Work with biostatisticians and clinical teams to clarify project needs and implement statistical analyses accurately
- Draft and review statistical analysis plans and programming specifications in line with regulatory expectations
- Maintain data quality and comply with applicable industry standards, including ICH/GCP guidelines, throughout programming activities
- Contribute to clinical study reports and other materials submitted to regulatory authorities
- Produce high-quality statistical programming deliverables in collaboration with project stakeholders and colleagues
Cerințe
- Bachelor’s degree in statistics, computer science, mathematics, or a related field
- Demonstrated clinical-research experience as a statistical programmer, including a strong understanding of statistical methods
- Working knowledge of SAS, R, or Python and experience with clinical data management systems
- Strong analytical and problem-solving abilities, careful attention to detail, and the capacity to work independently or collaboratively
- Clear communication skills, including the ability to explain complex statistical topics to non-technical stakeholders
- Legal authorization to work in the country where the position is located
Beneficii
- Base salary with performance-based incentives
- Health and wellbeing programs, including medical, dental, and vision coverage where applicable
- Retirement and pension programs
- Life assurance and disability coverage
- Employee assistance programs and wellbeing resources
- Professional development through structured training and career progression pathways