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.
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
Communicate with project teams and company departments with regard to statistical programming of clinical research projects
University degree in applied science, mathematics, statistics or similar
Strong knowledge of and experience with SAS software
Good knowledge of programming logic, SQL and macro programming is preferred
Full proficiency in English, spoken and written
Previous experience working with clinical trials
Good analytical skills
Proficiency in standard MS Office applications
Excellent communication and interpersonal skills
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.
Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way. We will guide and support you with information, making your experience as smooth as possible.
Please submit your CV in English.