Hi, How are you? Please find below the requirement and let me know if you have any consultants available.
Position: Statistical Programmer SAS Location: Danbury, CT Duration: 12 Months *Please respond with resumes at ksreed...@syergygbl.com <ksreed...@syergygbl.com>* Description: Supports the clinical research development process by providing statistical programming for new substances, indications or marketing claims. Works directly with the trial or project statistician and proactively with the Clinical Trial or Project team providing programming support. Implements and supports standards and a harmonized approach to programming. At the trial level, close collaboration with the Project Programmer is required to ensure project standards are implemented to support project reporting efficiently and effectively. Closely collaborates with other programmers to ensure the goals and timelines for the company is met. Skills: 1 - 3 years exp supporting clinical trials MS Biostat - Advanced SAS Certification required - can be verified via the Public Registry of SAS Certified Professionals. Education: Bachelors Degree or experience -- You received this message because you are subscribed to the Google Groups "REQSRESUMES" group. To unsubscribe from this group and stop receiving emails from it, send an email to reqsresumes+unsubscr...@googlegroups.com. To post to this group, send email to reqsresumes@googlegroups.com. Visit this group at https://groups.google.com/group/reqsresumes. For more options, visit https://groups.google.com/d/optout.
