Job: Statistical Programmer at Noymed LLC Company

Location: JobParser.Models.LocationModel

Category: Information Technology

Type: Full Time

Deadline: 02-Jul-18 00:00:00

Salary: N/A

Description
Are you looking for a place that appreciates your quality and dedicated work?
Do you want to be a better professional than yesterday? If yes, then NoyMed is the right place for you!

At NoyMed we believe we can grow only with our employees, therefore we demand and support professional growth of our talented team.
NoyMed LLC is looking for enthusiastic and energetic individuals to join our growing Biometrics team.

After 1 month training program the best candidates will be recruited to work at NoyMed (those candidates who have sufficient experience in statistical programming will be recruited without training).

Responsibilities
-Develop specifications for analysis datasets in consultation with Biostatistician
-Follow the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for SDTM datasets
-Follow statistical analysis plans and the Analysis Data Model (ADaM) Implementation Guide, writes specifications for analysis datasets
-Follow specifications, develops algorithms and writes programs to create datasets
-Develop the programs using SAS to produce Tables, Listings, and Graphs as per the specifications indicated in Statistical Analysis Plan
-Independently check data listings, summary tables and graphs
-Import and export SAS data
-Assist data management group in performing data edit checks
-Understand and conduct work consistent with GCP, ICH, 21 CFR part 11, internal SOPs and trainings, and international regulatory requirements
-Interacts with the project statistician and guides other programmers participating on a project team

RequiredQualifications
-Bachelor degree in Computer Science or related field with 3-6 years related experience
-In-depth understanding of data collection, data flow management, data quality, data extraction and data standards (knowledge of CDISC standards for CDASH, SDTM and ADaM a plus)
-Experience with multiple programming languages (SAS programming language, R, SQL or other languages/tools as required, SAS Certification desired), including the creation of data entry and query screens/processes and data quality checks
-Experience in reports and query development, especially for data validation and data quality assessment; experience with electronic data capture (EDC) and database management systems (e.g., REDCap, Velos, Medidata, TrialMaster, Inform, etc.)
-In-depth knowledge of research processes, clinical operations, and data quality management
-Strong attention to detail and demonstrated proficiency in quantitative and qualitative analyses
-Ability to manage multiple projects, tasks, and priorities; work independently with minimal supervision and execute tasks to completion without a great deal of direction
-Experience in training users in operation of clinical trials software and tools
-Ability to exercise judgment, initiative, and resourcefulness in making decisions in consultation with clinical research personnel, and independently if necessary
-Demonstrated strong teamwork and organizational skills; outstanding interpersonal and communication skills

Benefits

Job URL: iJob.am - Statistical Programmer @ Noymed LLC