Hello,


We are a Product Development & Data Science Company with Delivery Centers
in Michigan and Ohio And Offshore Delivery Centers in Hyderabad, India. We
also have a substantial Consulting team. Please visit us at
www.ntc-us.comfor additional information.



Enclosed is a list of our current openings. Please respond to this message
or contact us using the below mentioned information for further details.




*Title: SAS Programmer Duration: 6+ Months Location: NJ, MA, CA, CT*

These are SAS roles that will be working out of our NJ, MA, CA and CT
offices. Please send me any qualified candidates you may have .
A brief description of the responsibilities is below:
Ø Create submission-ready standard data presentations and data sets using
standard coding and following standard industry processes including SDLC
Ø Creating SAS programs and producing outputs to support the analysis and
reporting of clinical trials.
Ø Developing analysis datasets for trial level reporting by following the
Analysis Data Model (ADaM).
Ø Programming standard and custom data listings, summary tables, and graphs
as specified in statistical analysis plan
Ø Extract the data from clinical database for data reporting purpose.
Ø Develop programming specifications by analyzing the protocol related
documents. Meet the programming requirements for submissions as required
Ø Understand and plan work to delivery timelines including allowing time
for internal QC, as appropriate
Ø Whenever required, collaborate with the statistician, data managers, and
clinicians to resolve specifications and data related issues.
Ø Work with supervisor to balance conflicting priorities
Ø Understand timelines for and milestones affecting their work and alert
supervisor and client representative to potential slippage
Ø Run routine QC programs, track the changes in programming and
specifications, and document the QC results and resolutions.
Ø Carry out rework as requested by supervisor or client representative
Ø Follow escalation process and neither suppress nor over- escalate issues
Ø Contribute to close –out evaluations and any discussion
Ø Ensure compliance with Eliassen and industry quality standards,
guidelines and procedures
Ø Other duties as assigned.

Professional/Technical Skills & Experience:
Ø Experience of extracting, manipulating, summarizing, analyzing and
presenting data using SAS procedures
Ø Experience of SAS programming, Macro development, SQL and SAS/Connect
procedures. Strong knowledge of reporting procedures like proc report, proc
summary, and proc tabulate.
Ø Strong knowledge of SAS/GRAPH and Statistical procedures related to
SAS/STAT
Ø Ability to validate SAS programs that produce derived-analysis datasets
and data analyses
Ø Some experience in preparations for NDA filings. Thorough understanding
of regulatory guidelines like Good Clinical Practices (GCP), ICH
guidelines, 21 CFR part-11 compliance requirements.
Ø Knowledge of coding dictionaries (WHO, COSTART, ICD-9, MedDRA) expected
Ø Knowledge of CDISC® related data models like SDTM, and ADAM.
Ø Proficiency in Microsoft Office Applications
Ø Excellent verbal and written communication skills
Ø Detail oriented, ability to multitask with strong prioritization,
planning and organization skills
Ø Excellent team player






*Please fill all the below details  !!!*

*Full Name:  *

*Email:                                                   *

*Phone: *

*Visa: *

*Availability: *

*Relocation: *

*Current location: *

*Skype ID: *





*Please provide me two official references from your recent project :*

*Name of candidate:*

*Job role:*

*Official Mail ID:*

*Contact Number:*

*Client Name:*



*Name of candidate:*

*Job role:*

*Official Mail ID:*

*Contact Number:*

*Client Name:*







Best Regards,

*Sandeep*

*Neumeric Technologies *

Email: [email protected]

Yahoo:  sandeep_abcd567

Visit us at www.ntc-us.com for further details



*Oracle Gold Partner | Microsoft Partner | IBM Partner*

*-- Ask us about our $500 referral fees/incentive policy --*

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