Innovations technological

Hi,

 

Hope you are doing well..!

 

This is Sunil from Iqlabs Inc.. Please find the job description below, if you are interested please reply my email or even reach me on my number 510-509-7998.

Need copy of Visa and two references

 

Title: SAS Programmer

Number of Positions: 1

Location: Holliston, MA

Duration: 6 Months +

Interview: Personal Preferred

Visa: H1/EAD/GC/USC

 

Description:

 

Working under the direction of the Biostatistician or senior SAS programmer, the SAS

programmer conducts programming activities for a trial, early phase project, indication,

or publication activities. Develops and supports statistical programming computer

systems that are used in the production of statistical analysis plan (SAP)-planned tables,

data listings, and graphs, integrated summaries of safety and efficacy, ad hoc analyses

and electronic submission deliverables, such as datasets, data documentation, programs,

programming table of contents, and patient profiles.

 

Essential functions include creating systems that assist the biostatistical programming

staff and biostatistical staff to create tables, data listings, graphs, and analysis for final

reports, abstracts, posters, manuscripts, and other clinical publications; developing

systems to support electronic regulatory submissions; providing systems and support for

clinical data management staff, clinical programmers, quality control (QC) staff, and

biostatisticians; producing and supporting systems that extract data from the clinical

database; and building analysis databases composed of SAS datasets.

 

The SAS programmer must follow established standardized design and programming

procedures; assist in establishing standardized programming procedures and work

instructions; develop, enhance, evaluate, and validate standardized macros and utility

programs; ensure that regulatory requirements are met through validation/compliance

activities; and develop and maintain clinical processing work flow systems.

 

Minimum Requirements

 

• BS or MS degree in Computer Science, Computer Information Systems,

Statistics, or related health science field with a minimum of 1 year of SAS

programming experience with clinical trial data.

• General knowledge of regulatory requirements and drug development process.

• Excellent organizational skills and good verbal and written communication skills.

• Ability to work independently is required.

 

Requirement 2:

Title: Senior SAS Programmer

Number of Positions: 1

Location: Holliston, MA

Duration: 6 Months +

Interview: Personal Preferred

Visa: H1/EAD/GC/USC

 

 

Description:

The Senior SAS programmer leads the programming activities for a trial, early phase

project, indication, or publication activities. Develops and supports statistical

programming computer systems that are used in the production of statistical analysis plan

(SAP)-planned tables, data listings, and graphs, integrated summaries of safety and

efficacy, ad hoc analyses and electronic submission deliverables, such as datasets, data

documentation, programs, programming table of contents, and patient profiles. In

addition, the Senior SAS Programmer supports migration activities in the creation of

Standard Data Tabulation Model (SDTM) and production of the Analysis Data Model

(ADaM). This Senior SAS Programmer is also responsible for monitoring and meeting

assigned program milestones and may lead a small team of statistical in-house or

consultant programmers to accomplish tasks.

 

Essential functions include creating systems that assist the biostatistical programming

staff and biostatistical staff to create tables, data listings, graphs, and analysis for final

reports, abstracts, posters, manuscripts, and other clinical publications; developing

systems to support electronic regulatory submissions; providing systems and support for

clinical data management staff, clinical programmers, quality control (QC) staff, and

biostatisticians; producing and supporting systems that extract data from the clinical

database; and building SDTM and Adam compliant databases composed of SAS datasets.

The senior SAS programmer must follow established standardized design and

programming procedures (CDISC); provide mentoring to junior level SAS programmers;

assist in establishing standardized programming procedures and work instructions;

develop, enhance, evaluate, and validate standardized macros and utility programs;

ensure that regulatory requirements are met through validation/compliance activities; and

develop and maintain clinical processing work flow systems.

 

Minimum Requirements

 

·         BS or MS degree in Computer Science, Computer Information Systems,

·         Statistics, Engineering or related health science field with a minimum of 2 years

·         of SAS programming experience with clinical trial data.

·         Good working knowledge of CDISC SDTM Implementation Guidelines.

·         Good working knowledge of CDISC ADaM Implementation Guidelines.

·         General knowledge of regulatory requirements and drug development process.

·         Excellent organizational skills and good verbal and written communication skills.

·         Ability to work independently is required.

Name
Primary Skills
Current Location
Best Time to attend Telephonic Interview
Contact No
E-Mail
Rate
Visa Status
Availability
Willing to Relocate
Total Exp
US Exp.
References from last 3 projects with official email ID and contacts numbers Note:  References will be used if interview is successful.
Education (Highest Degree and year)
SSN Last Four Numbers
Date Of Birth

 

 

 

Thanks & Regards

-----------------------

Sunil Kumar. P

sunil@iqlabs.net

510-509-7998

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