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We are a dynamic and global company that values our staff, clients, partners, and the quality of work we do. As a leading Contract Research Organization (CRO), we bring together over 2,700 driven, dedicated, and passionate individuals who work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Key Responsibilities- Contribute to statistical programming activities related to global clinical trials, working closely with international teams of statisticians, programmers, and data managers.
- Develop analysis data sets structure and program requirements and specifications.
- Be involved in SAS programming of ADS and Tables, Listings, and Figures, and support SAS program validations.
- Prepare and review program documentation, produce TFL, and communicate with project teams and company departments regarding statistical programming of clinical research projects.
- University and master's degree in applied science, mathematics, statistics, or a related field.
- Knowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) and experience working in the SAS system.
- Good knowledge of programming logic, SQL, and macro programming is preferred.
- Proficient in English, spoken and written.
- Experience within clinical trials and/or biostatistics.
- Good analytical skills and proficiency in standard MS Office applications.
- Excellent communication and interpersonal skills.
Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors. We strive to be a well-respected, global company that values its employees, clients, and partners. We are committed to delivering high-quality services and making a positive impact in the lives of those we serve.
