March 26, 2014

{Job Junction} Urgent Need : Sr Clinical SAS Programmer in Woodcliff Lake, NJ ***NEED LOCALS ONLY

Hi

Please send profiles to Richard@svksystems.com

 

NEED LOCALS ONLY

Face to Face After Telephonic

 

Title : Sr Clinical SAS Programmer in Woodcliff Lake, NJ

Duration : 12 Months

 

Duties:

To Support the Oncology Data Management group by carrying out the following functions:

·         Work independently to provide complex data review Listings, Reports, Patient profiles and Edit checks for Clinical and DM team.

·         Participate in review process of study documents such as the annotated CRFs/eCRFs.

·         Design and develop SAS macros, small applications, and other utilities to expedite SAS programming activities and usage by the Oncology Data Management and other areas of Clinical for data review.

·         Develop and maintain the standard programs and Macro Libraries along with the related documentation.

·         Develop standard programs and macros to convert raw data into SDTM data along with the Define.xlm file.

·         Lead the assign project with minimum guidance and with proper documentation.

·         Ensure all programming activities and processes performed are conducted according to standard operating procedures and good programming practice.

 

QUALIFICATIONS:

·         Minimum of Bachelor’s degree in Statistics, Computer Science, Mathematics or a related science discipline. But Masters preferred.

·         At least 8 years of experience in programming with clinical trial data and developing programs, testing, and documentation.

·         Strong SAS programming skills required in Windows and UNIX environment, with proficiency in SAS/Base, SAS Macros, SAS/Graph, & SQL.

·         Strong experience in handling SDTM data for programming.

·         Good experience for handling external data, e.g., laboratory data, PK, ECG, etc.

·         Good understanding of Data Management Process.

·         Good understanding of Oncology.

·         Good understanding of SAS system related programming.

·         Strong experience in handling standards specific to clinical trials, such as CDISC, SDTM, MedDRA, WHO DRUG.

·         Good understanding of relational databases, e.g., ORACLE; Knowledge of the EDC System, InForm and underlying data structure is a plus.

·         Knowledge of using JReview is a plus.

·         Strong problem-solving skills.

·         Able to lead projects, work independently, and a team player; Good organizational and time management skills.

·         Capable of communicating technical concepts.

·         Good understanding of system development life cycles, GCP, and related Regulatory guidelines.

 

Thanks & Regards,


Richard
SVK Systems Inc
11465, Johns Creek Parkway, Suite #180, Johns Creek, GA - 30097
Contact: 678-824-7780 | Fax: 404-601-9507

Email: richard@svksystems.com | Gmail: richard05svk@gmail.com

Website: www.svksystems.com

Description: Description: Description: Inc.500|5000 Logo Description: Description: Description: cid:image001.png@01CD0200.91BFE3E0Description: Description: Description: http://t0.gstatic.com/images?q=tbn:ANd9GcSQsCTiUiVCUIlXuZilZE964QZGU0mixwsOAsuJRxcUzIIa6rlVRKKhTw Description: Description: Description: http://t1.gstatic.com/images?q=tbn:ANd9GcRQFqqr5LzMAumX3JTxImVUvRAUWAULRPdx3k2_neWeGv9jMnH_sJbboeoDescription: Description: Description: Description: Description: Description: Description: http://t0.gstatic.com/images?q=tbn:ANd9GcTzWHC3crnfdWlRitTOkW4JO_g6sndCgqKJs7hRRCKBTS1sG__j

 

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