Hi

Please send profiles to* rich...@svksystems.com <rich...@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: rich...@svksystems.com | Gmail: richard05...@gmail.com

Website: www.svksystems.com

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