Intego Group’s Biometric Department is expanding clinical research practice. We’re looking for bright individuals to join our growing team in Intego’s offices. You will be part of an extensive six-month training program provided by leading experts in the industry of clinical trials and will be responsible for all aspects of statistical programming and analysis of clinical trials data. As a Statistical Programmer, you will be responsible for accessing and assembling clinical data, creating derived datasets following industry and client specifications, generating tables, figures, and listings to support analysis.
The role of the Statistical Programmer is to use broad technical origramming and data analysis skills.You will perform data analysis to support different clinical trials activities using SAS®, R, SQL, and other modern tools.
Applying modern statistical methods to clinical data, you will support quality control, regulatory submissions, marketing research, and strategic decision-making with close interactions with clinical study teams. General responsibilities include:
The successful candidate will possess at least one of the following qualifications:
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At Intego Group, we value all employees and job candidates as unique individuals, and we welcome the variety of experiences they bring to our company. As such, we have a strict non-discrimination policy. We believe everyone should be treated equally regardless of race, sex, gender identification, sexual orientation, national origin, native language, religion, age, disability, marital status, citizenship, pregnancy, or any other characteristic protected by law.