Associate Statistical Programmer

Catalyst Clinical Research provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology, a full-service oncology CRO, and multi-therapeutic global functional and CRO services through Catalyst Flex. The company's customer-centric flexible service model, innovative technology, expert team members, and global presence advance clinical studies. Visit CatalystCR.com.

Job Description

4-Oct-24 Confidential

JOB Title: Associate SAS Programmer

Job summary:

Develop SAS programs to produce high quality deliverables within set timelines in accordance with company and regulatory requirements.

Key activities:

• 
  Use additional statistical packages like R, or other high-level programming languages as

appropriate.

• 
  Generate customized reports using PROCREPORT techniques

• 
  Involve in Statistical programming and validation of Analysis Datasets and Tables,

Listings, Graphs (TLG'S)

• 
  Knowledge of CDISC services and hands on experience in developing SDTM datasets.

• 
  Work closely with team, Statistician and prepare adhoc reports for analysis.

• 
  Basic knowledge on SAS macros and ProcSQL.

• 
  Understand Study specific documents like Protocol, SAP and give presentations.

• 
  Understand all SOP’s as part of the organization and ensure to adhere to all the rules and

responsibilities.

• 
  Develop numerous SAS programs with the help of SAS Statistical Procedures such as

ProcMeans, ProcTabulate, ProcFreq, Proc Summary.

Qualifications:

• 
  MSC in Statistics and Effective Communication Skills.

• 
  0 - 1year of experience, or an equivalent combination of education or experience

• 
  Good understanding of Clinical Trials and the various terminologies