Skill: clinical study , ich-gcp; Exp: 0-3 years; The Statistical Programmer I works with supervision to support various programming activities related to the analysis and reporting of clinical study data. QualificationsExcellent analytical skills. Knowledge and understanding of the programming and reporting process. Knowledge of SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11. Ability to learn new systems and function in an evolving technical environment. Attention to detail. Ability to successfully work as part of a global team. Work effectively in a quality-focused environment. Effective time management in order to meet daily metrics or team objectives. Show commitment to and perform consistently high quality work.
Function: Biotech / Pharma / R&D