Target Health Inc. is a full-service Contract Research Organization and Clinical Trials Software company, serving the biopharmaceutical and medical device industry.
We are committed, through creative collaboration, to serve the life sciences community with knowledge, experience, technology and connectivity. Our pledge is to optimize the life cycle of drugs, biologics and devices with expertise, leadership, innovation and teamwork.
We provide superior, consistent performance with a cutting edge, diverse team with the highest standards of ethical conduct and integrity.
Do you have what it takes to join our diverse, high performing team?
Design, code and debug SAS programs using SAS (BASE/STAT); Analyze and coordinate SAS programming activities supporting Clinical Data Management, eCRF development, biostatistics in clinical trials using Linear Model,T-test/chi-square test, and Multivariate analysis; Create statistical tables, summaries and listings for clinical trial data analysis using Hypothesis testing, Analysis of variance (ANOVA); Write and execute SDTM mapping programs, Data Management Plan,Data Transfer Specifications and Data Validation Plan documents; Create, retrieve, update and manage raw data using Database management systems (DBMS); Participates in the validation/QC of SAS programs, analysis datasets and data entry.
Must have a Master’s Degree in Statistics, Applied Mathematics and Statistics, or Biostatistics plus skills and knowledge in SAS (BASE/STAT), Data Analysis, Linear Model, Multivariate analysis, Chi-square test, Hypothesis testing, Analysis of variance (ANOVA).
New York, NY
Send resume with job code SAR002 to HR, Target Health, Inc., 261 Madison Ave, 24th Floor, New York, NY 10016.
Provide statistical support for study design, data transfer, analysis, verification, interpretation of results in clinical trials. Program datasets used for analysis according to CDISC standard, along with data define documentation and data reviewer’s guide. Create and verify listings/tables/figures based on data collected in clinical trials. Work closely with data management, clinical and regulatory departments.
Master's degree in Statistics or Biostatistics, Good programming skills and knowledge of SAS, and familiar with CDISC, 1 to 3 years’ experience in the industry is a plus.
New York, NY
Please apply through one of the following:
Please note: Agency candidates are not accepted at this time.