We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,200 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
You will contribute to statistical programming activities related to global clinical trials, work closely with international teams of statisticians, programmers and data managers, program data sets and summaries.
This is a Home-Based role located in the United States.
You will: * Develop analysis data sets structure * Develop program requirements and specifications * Be involved in SAS programming of ADS and Tables, Listings and Figures * Support SAS program validations * Prepare and review program documentation * Produce TFL * Communicate with project teams and company departments with regard to statistical programming of clinical research projects
Qualifications * University degree in applied science, mathematics, statistics or the like * Minimum 5 years of experience in the clinical research industry (CRO experience preferred) * Knowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) and experience of work in SAS system * Good knowledge of programming logic, SQL and macro programming is preferred * Experience within clinical trials and/or Biostatistics * Good analytical skills * Proficiency in standard MS Office applications * Excellent communication and interpersonal skills
Join our highly dedicated team of clinical research professionals and make a tangible difference within a professional and energetic organization founded by scientists.
All your information will be kept confidential according to EEO guidelines.