A new Job, ID: 200814 <http://ejobsville.com/display-job/200814> was added
at eJobsVille.com - For the Best Tech Jobs in Town <http://ejobsville.com/>

Title:  Statistical SAS programmer  posted on 2014-07-02 19:19:43

Job Description:Hi,
Greetings for the day!
This is Suresh from Paradigm info tech; I am working with following
requirement. Please help me with updated resumes ASAP…………………
Position         : Statistical SAS programmer.
Location           : Woodcliff Lake, NJ

*Job description*:








*Biostat programmerOncology PCUTo support the Biostatistics team by
carrying out and overseeing programming activities of statistical
programmers and external vendors (as required), and to ensure timely and
accurate programming and validation activities for clinical studies.
Contributes to the overall efficiency and best practice running of the
Biostatistics group, demonstrating the ability to work efficiently and to a
high standard within a clinical team environment.Main
duties/responsibilities:1. Providing statistical programming and validation
support for clinical study reports, overseeing programming activities by
external vendors (e.g., CROs) when necessary and coordinating programming
activities among the study programmers to achieve timely progress in the
following areas: analysis datasets, statistical tables, figures, listings,
Integrated Summaries of Safety (ISS), Integrated Summaries of Efficacy
(ISE), electronic submissions and other internal and external requests
(e.g., publications). Accessing and converting data to SAS from Database
management system and PC file formats (e.g., MS Excel, text files). Working
with external vendors in order to develop or monitor the content and
structure of SAS data sets.2. Developing and maintaining SOPs, SWPs and
other related technical documents, providing input to the Database and CRF
Development, creating edit check programs and providing feedback to the
Data Management. Providing input in developing statistical analysis plans,
specifications of analysis datasets, validation plans, and other related
documents. Determining and researching SAS software upgrades and related
systems and addressing maintenance issues. *














*3. Managing and developing team, maintaining standards for programming
activities, and guiding/coaching Statistical programmers.4. Working
independently to accomplish tasks and goals defined by supervisor.
Attending required training and meetings and bringing in new ideas to
improve the programming process.* Responsibilities weighting may change
significantly based on the incumbent and their assigned areas of
responsibility.Qualifications and education required:• Minimum of
Bachelor’s degree in Statistics, Computer Science, Mathematics, or a
related science discipline. Masters preferred.Experience required: *


*• Minimum 5 years experience in SAS programming for phase I-IV clinical
trials in a pharmaceutical/CRO environment. 7+ years experience preferred.•
Some project experience in a pharmaceutical/CRO programming environment or
demonstrated significant leadership of SAS programming activities in a
clinical pharmaceutical/CRO environment. *





*Skills and aptitude required:• Experience using SAS-Base, MACRO, STAT,
GRAPH, ACCESS, MS Office. *




*• Proven experience with Unix and Windows operating systems.•
Understanding of the software development life cycle.• Understanding of FDA
guidelines.• Good organization, time management and attention to detail
skills needed to work in a stressful environment under tight deadlines
while maintaining focus on details and quality.• Applies good judgment and
demonstrates initiative to resolve issues. *
*• Strong verbal, written and interpersonal communication skills needed to
work effectively in a team environment, managing that team as required.*




*Click here to view full job description and apply
<http://ejobsville.com/display-job/200814>  (Registration not mandatory to
apply for this job)*

------------------------------
Best regards,
eJobsVille.com - For The Best Tech Jobs In Town

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