SAS Programmer - Clinical Trials

Hiringlink Solutions
  • Bangalore
  • 10-15 lakh
  • 5-15 years
  • 27 Aug 2015

  • Production/ Manufacturing/ Engineering

  • Pharmaceuticals/ Life Sciences/ Clinical Research
Job Description

The programming, testing, and documentation of programs for use in creating statistical tables, figures and listing,

* The programming of analysis dataset (derived datasets) and transfer files for internal and external clients. and

* The programming quality control checks for the source data and report the data issues periodically.

* Detect errors in detail, corrects them (e.g., reviews tables/listings, edit checks output and SAS programs to ensure quality of deliverable) and report it to appropriate personals (internal or external clients)

* Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams and Statistical Programming department.

* Perform and plan the development, implementation and validation of new process technologies, macros and applications.

* Fulfill project responsibilities at the level of technical team lead for single studies, under supervision.

* Understand timelines for and milestones affecting their work and alert supervisor to potential slippage.

* Provide training and mentoring to SP team members

* Knowledge of statistics, programming and/or clinical drug development process

* In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

* Working knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language

Competencies/Skill sets for this job


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