Wednesday, February 24, 2016

{SAP JOBS USA:160791} Urgent Requirement :: Senior Statistical Programmer ::South SF, CA :: 6+months :: Phone/Skype

Hello,
 
Hope you are doing good!
This is very urgent opening. Please send your available matching candidates on
dhruv@riderconsultinginc.com

 
Role: Senior Statistical Programmer

Location: South SF, CA

Duration:  6+months
Interview: Phone/skype

 

Description:

·         Senior Statistical Programmer

·         SAS® programming to provide programming support for multiple oncology studies in multiple stages of clinical development.

·         This role will interact with Biostatistics, Clinical Data Management, Medical Writing, Clinical Information Systems, Clinical Operations, Drug Safety, Regulatory and Medical to design, write, and validate SAS® programs in accordance with company, industry, and regulatory requirements.

·         We need for a senior level statistical programmer (at least 10 years industry experience.)  The candidate have be strong SAS skills and good communication skills. Knowledge of CDISC experience in oncology are desirable but not required.  The candidate must work on site in South San Francisco, CA. This is a six month contract that's extendable or could be converted to FTE if it is the candidate preference.

 

Responsibilities:

·         Develop and validate SAS® programs to produce high quality deliverables within set timelines in accordance with company and regulatory requirements. The deliverables include SDTM and ADaM datasets, tables, listings and figures.

·         Review and provide feedback on deliverables from other clinical groups including but not limited to: statistical analysis plans; table, listing, and figure shells; data management plans; data transfer plans; Safety Report Specification; electronic data entry screens; and case report forms.

·         Clear and proactive communication with Study and Project teams to clarify requirements and specifications, update others on assignment status, and to convey data irregularities.

·         Create and validate global macros or systems that streamline repetitive operations to increase programming efficiency.

·         Keep abreast of SAS enhancements.

·         Have excellent verbal and written communication skills and interpersonal skills.

·         Have good knowledge of clinical trial study design and electronic data submission requirements.

·         Provide active support on initiatives that facilitate infrastructure and process enhancements within Biometrics.

 

Requirements:

·         Proficient in SAS.

·         BS or equivalent relevant education and 5+ years or MS/PhD and 2+ years of software development and/or programming experience; years of experience may substitute for education.

·         Experience implementing CDISC standards.

·         Collaborative and positive attitude.

·         Good written and verbal communication skills.

·         Good knowledge of Unix/Linux desirable.

 

 

Dhruv Soni, 

Sr. Technical Recruiter

T:218-656-0390 

dhruv@riderconsultinginc.com
Rider Consulting Inc  |  50 Craigwood rd, suite 205, South plainfield, New jersey | www.riderconsultinginc.com

 

 

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