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Associate Statistical Programmer at Catalyst Clinical Research
Thiruvananthapuram, kerala, India -
Full Time

Start Date

Immediate

Expiry Date

08 Feb, 26

Salary

0.0

Posted On

10 Nov, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

SAS Programming, Statistical Programming, R, CDISC, SDTM Datasets, Statistical Procedures, ProcMeans, ProcTabulate, ProcFreq, Proc Summary, Effective Communication, Clinical Trials, Adhoc Reports, SOPs, Presentation Skills, Data Validation

Industry

Research Services

Description
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
Responsibilities
Develop SAS programs to produce high quality deliverables within set timelines. Involve in statistical programming and validation of analysis datasets and reports.