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Sponsor Address

Westchester NY

Position Title

Sr. SAS Clinical Programmer

Number of Positions

1

Why is the position open?

Growth

Sourcing Preferences

Directly from industry

Knock Out Factors

 

Personality Desired

culture fit

Background of the last 2 Hired

Directly from the industry, from Pharmaceutical, Biotech, CRO

How long Open

 

Employee needed by

  

Number of Interviews

2-6

Who Else Interviews

interdepartmental

Salary

$80-$90

Bonus

20%

First Year Income

$90+

Benefits

full package

Vacation Time

full

Who does the person report to

Head of Department

Position Leads To

possible project lead, or management

Position Selling Information

Company has strong growth, great products and a strong career-oriented culture

Other Sources Employer Using to Hire

na

Exclusive

no

 

Job Order Requistion

Date of Request

 

Position Title

Sr SAS Clinical Programmer

Location (Town, Region)

Westchester NY

Employment Type

full time

Travel %

none

Travel Locations

none

Therapeutic Area

variety

Start Date

immediate

First year income

$90+

Degree Required

BS 4 yr MS Sciences or Mathematics preferred

Years of professional and related experience

5=

 

Requirements

Bachelor's degree required. Master's degree would be helpful. Minimum three (3) years of relevant SAS programming in a biotechnology or pharmaceutical company. SAS Certification desirable. Knowledge of statistics a must as well as SAS procedures

 

 

 

Duties and Responsibilities

Works independently to design and test program logic, coding programs, program documentation and preparation of programs for computer operations. Oversees projects designed to support ongoing clinical studies requests for statistical and non-statistical analyses. Meets statistical adhoc requests of senior management. Provides documentation and consistent maintenance of code, logs, and outputs in a regulated environment.

Duties and Responsibilities include, but are not limited to, the following:

-Indentifies data quality issues, and recommends and implements solutions to resolve those issues
-Develops sophisticated analytics and data modeling in support of clinical trials
-Integrates data from various sources for use in validating trials
-Documents and validates results generated
-Communicates data results of Clinical departments
-Generates assorted tables and analyses as required for internal and external use
-Writes SOPs pertaining to statistics and data management
-Writes and checks codes written by SAS Statistical Programmer(s) to be used for statistical programs and performs quality control checks to ensure codes work according to program design
-Reviews table figures set-up look for inconsistencies and correct if any are found
-Sets program adhoc report runs based on department and reporting needs
-Interacts frequently with members of Clinical team on adhoc requests of senior management