~~ Technical Recruiters Network ~~ Hot Job for the position of SAS Clinical Programmer @ San Francisco/CA

Hi Associate,

Currently, I am recruiting candidates for one of my requirement as mentioned below. If you have a matching profile, please send me the updated resume along with contact details at the earliest.

Job Title	SAS Clinical Programmer
Project Location	San Francisco CA
Duration	6 months /Contract

 
Skills Required and Job Description:

Responsibilities: Assist in the review of key study-related documents produced by other functions, e.g. SAP, case report form, data management plan, database specifications, EDC data structures, DMC plans and other clinical documents. Write, test and validate SAS programs to produce analysis datasets, TLGs and presentation output, to be included in reports for submission to regulatory agencies, publications and other communications Write CDSIC standard dataset specifications and follow specifications to create SDTM and ADAM datasets. Understand and execute department-, product- and study-level macros and utilities. Write, test and validate product- and study-level macros and utilities. Provide input to and participate in intra-departmental meetings Contribute to the continuous improvement of Statistical programming group. Assist in the review of Statistical Programming policies, standard operating procedures and other controlled documents. Provide support to and mentor junior programmers and contractors Interface with outsourcing partners and vendor. Attend external professional organizations, conferences, training and/or meetings  Knowledge: Computer programming using SAS Understanding of computer operating systems, word processors, document applications Fundamentals of project planning and management Drug development process Preferred Qualifications: Bachelors or Master’s degree, in Computer Science, Statistics, Mathematics, Life Sciences or other relevant scientific subject 8+ years clinical research and development statistical programming experience using SAS Extensive hands-on experience in developing CDSIC standard specifications and datasets (SDTM, ADAM) Experience in Oncology Trials Experience in FDA/EMEA trial submissions Drug Development (pre-, early, late and/or observational) in related industries or academic research

Note: Please use update button on top of this email to upload your hotlist so that we don't send you unwanted Reqs. 

Thanks & Regards,

 

Sandeep Kumar

(Technical Resource Specialist)

.......consulting redefined Ramy Infotech, Inc

Renaissance Business Center, 1851 McCarthy Blvd, Suite 107, Milpitas, CA 95035

Phone : 408-317-9256 EXT :331

Fax : 408-273-6834

Email : sandeep.kumar@ramyinfotech.com

URL : www.ramyinfotech.com

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