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Urgent! Clinical SAS Programmer Job Opening In Hartford Connecticut – Now Hiring Katalyst Healthcares & Life Sciences

Clinical SAS Programmer



Job description

Responsibilities:


  • Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s).


  • Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets.


  • Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements.


  • Provides input in the design and development of case report forms and clinical databases.


  • Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs.

  • Programs quality checks for clinical study raw data and report the findings to Data Management.


  • Provides input in the design and development of case report forms and clinical study databases.


  • Reviews or author eCRF, SDTM and ADaM datasets specifications for datasets programming.


  • Provides programming support for adhoc analysis.


  • Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group (e.g., macros or graphical user interface applications).


  • Manages timelines and schedules of specific phases of projects with internal personnel and external vendors.


  • Acts as lead programmer for a study.


  • Reviews or validates statistical deliverables of vendors for assigned project(s).




Requirements:




  • MS in Statistics, Computer Science, or a related field with at least 3 years or BS in Statistics, Computer Science, or a related field with at least 5 years.


  • Experience in providing statistical programming support to early and late phase clinical trials.


  • Excellent skills in SAS programming and statistical reporting.


  • Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements.


  • Familiarity with FDA and ICH regulations and guidelines.


  • Excellent problem-solving skills.


  • Good written and verbal communication skills and organizational and documentation skills.


  • Ability to work on a multidisciplinary team that may include Biostatistics, Medical Directors, Data Management, Medical Writing, Pharmacovigilance, Clinical Operations, Medical Affairs, etc.


  • Ability to prioritize and multi-task effectively.


  • Demonstrated positive attitude and the ability to work well with others.








Required Skill Profession

Other General



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