Job Description

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.







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