Sr Stats Programmer

CDISC, statistical SAS
Full Time, Part Time, Contract Corp-To-Corp, Contract Independent, Contract W2, C2H Corp-To-Corp, C2H Independent, C2H W2, 6 months

Job Description

Job: Sr Stats Programmer

Location: San Francisco, CA(This position will start out remote, but candidates must be willing to relocate to if COVID19 restrictions are lifted.)

Duration: 6+ months

Interview: Phone / Face-to-face or Skype to start

Job Description:

Primary Responsibilities

Independently program CDSIC SDTM, ADaM datasets and to ensure submission requirements are met

Develop define.xml and RGs for submissions

Develop Tables, Listing and Figures per the SAP, DMC, or annual Safety report specifications

Validate and QC SAS programs as needed

Provide validation support for programming tasks that are required for posters and publications

Work on multiple tasks and prioritize tasks to meet the needs

Understands importance of timelines and strives to meet them at all times

Proven ability to prioritize tasks, delegate or escalate as needed

Must Have/Required

B.S. degree in computer science, statistics, mathematics or related areas and 6+ years of direct and related experience in pharmaceutical and biotechnology industry

A very clear and proven hands-on experience with safety annual reports, integrated analyses familiarity with IND/BLA electronic submission requirements is a plus

Proven ability to write cross-referencing check programs as needed

Familiarity with CDISC Standards including SDTM and ADaM

Strong SAS programming skills including macros and statistical procedures

Strong experience with SAS GRAPH and ODS output

Successful history and experience with CDISC standards and development

Excellent understanding of clinical trials and regulated and GCP compliant working environment

Excellent oral and written communication skills

Dice Id : 10423087
Position Id : 2020-2073
Originally Posted : 1 year ago
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