Description
If you have clinical research, biotech or pharmaceutical experience and you're looking for a company and career where your work can have an impact, we'd like to talk to youAs a Statistical Programmer you will provide specialized knowledge and support to carry out statistical and clinical programming activities in support of one or more clinical research studies.
Role:
In this role you will create/maintain tables/listings/graphs, using SAS; create specifications and programs for analysis, reformatted, and CDISC datasets. You will perform programming validation/QC checks, provide ad-hoc reports, and may assist in programming edit checks.
In this role you will work with multiple study teams and will maintain the full-scope of responsibility for assigned projects: ensuring on-time delivery, communicating the status of projects to internal teams.
Required Skills
Qualified candidates will have a Bachelor's degree or equivalent in mathematics, statistics, or related field of study. Degree and experience in Computer Science, Statistics, or related field. Candidates will have at least (3) years of biotechnology/pharmaceutical experience with a bachelor's degree or equivalent or at least three (1) years of pharmaceutical experience with a master's degree or equivalent or a Ph.D. degree with 2 years of experience.
Intermediate/Advanced knowledge of SAS, SPSS, or other statistical software required
Required Experience
Relevant experience includes comprehension of GCP and other industry relevant guidelines as well as working knowledge of medical terminology, clinical trial methodologies, and FDA/ICH regulations. Candidates will have a working knowledge and understanding of regulatory guidelines for the use of computer systems in clinical trials and proficient knowledge of the data and reporting requirements for clinical trials.
To find out more about Real please visit www.realstaffing.com