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Friday, 18 March 2016

Job description

PRIMARY RESPONSIBILITIES
  • Build SAS datasets from clinical database.
  • Develop SAS macros, templates and utilities for data cleaning and reporting.
  • Utilize SDTM guidelines to build datasets.
  • Communicate with an internal team to create deliverables for pharmaceutical and biotechnology clients.
  • Implement analyses specified in the protocol or the Statistical Analysis Plan (SAP) while working with the project statistician.
  • Ensure CRF meets the guidelines of the protocol and check for consistency and adequacy.
  • Write SAS programs to generate tables, listings, and figures and analysis datasets.
  • Review CRF annotations and data specifications.
  • Work in tandem with Biostatistics and Data Management member on various clinical projects.
  • Identify and edit checks per the data validation plan or data management plan.
  • Study management reports using SAS.
  • Validate the programmed analysis datasets, tables, listing and figures.
  • Perform analyses defined in the statistical analysis.
  • Prepare clinical and statistical summary reports.
  • Communicate with programming and statistics leads.
  • Utilize SAS programming skills within protocol team and perform all programming required for clinical trial analysis and reporting.
  • Perform quality control on final reports.
  • Develop SAS coding and table templates for preparing, processing and analyzing clinical data.
  • Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues.

Desired Skills and Experience

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
  • Working knowledge of a relational database
  • Good conceptual, organizational and communication skills
  • Flexible approach with a conscientious attitude
  • Ability to establish and maintain effective working relationships with coworkers, managers and client
Eligibility - Candidate should be SAS Certified

Apply


Interested candidates can send their Resume to naveen.alexander@quintiles.com
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