*Hi,*


Hope you are doing well !

My name is *Steven* and I am a Recruiter with *Infotree Services*. With
reference to your resume registered at *Monster.com*.

I have an urgent opening with me, which appears to be a potential match for
the client's requirement. I have listed the job description for your
reference.

Please let me know if you would be interested in this position.

If so, please send me a copy of your updated resume with contact details
and the best time to reach you.

I will appreciate your response at the earliest, as the manager tends to
move fast !



*Job Details** :*



*Job Title*

*Sr. SAS Programmer Analyst (2138) (C2C Considerable)*

*Project Location*

*Woodcliff Lake, NJ 07677*

*Duration*

*12+ months/Contract*



*Job Description** :*


C2C Accepted - SR. SAS - WRITING GENERIC SAS PROGRAMS

Sr. SAS Programmer Analyst
Perform SAS programming to provide data review complex listings/reports to
support *Data Management function for Oncology trials*.
Focus on candidate with experience in writing SAS tools and developing
generic SAS programs for clinical studies
Develop programs for patient profiles and ad hoc reports for data review to
support the clinical teams for Oncology trials.
Program data edit checks as necessary to facilitate Data Management's data
cleaning activities.
Design and develop SAS macros, 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 programs including testing and organizing the SAS
datasets, SAS programs and related documentation.
Ensure all programming activities and processes performed are conducted
according to standard operating procedures and good programming skills.

*Qualifications:*
Strong SAS programming skills required in Windows and UNIX environment,
with proficiency in *SAS/Base, SAS Macros, SAS/Graph, SAS/ SQL*.
*7-10 years* of experience in programming with clinical trial data and
preparing programming and test documentation.
Extensive experience of handling external data, such as lab data, PK, ECG,
Tumor, etc.
Experience with JReview is a plus.
Good understanding of standards specific to clinical trials such as *CDISC,
SDTM, MedDRA, WHODRUG.*
Good understanding of relational databases such as *ORACLE, Knowledge of
the EDC system, InForm*, and underlying data structure is a plus.
Knowledge of data management process, good understanding of data cleaning
process.
Strong problem solving skills
Able to 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.

*NOTE:*

we need someone with *writing macro and generic program experience*.
Candidates must be *capable of writing complex generic system* related
macros and have written any generic programs or macros during their work
experience


*Thanks & Regards,*

*Steven* - Technical Recruiter

*Phone *(Direct): 734-888-8174

*Email:* ste...@infotreeservice.com <st...@infotreeservice.com> | *Website:*
www.infotreeservice.com

*LinkedIn:*  https://www.linkedin.com/pub/steven-fernandez/104/956/240

*Hangout:* steven.usrecruiter | *Yahoo:* steven.usrecruiter

*Mailing Address:* 215 Ann Arbor Rd. Suite 304 Plymouth, MI 48170





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