HI Hope you are doing great!!
Please find the requirement below , If you find yourself comfortable with the requirement please reply back with your updated resume and I will get back to you or I would really appreciate if you can give me a call back at my contact number *408-317-9256 EXT:-336.* *Position: SAS Programmer* *Location: Berkeley Heights, NJ* *Duration: **6+ Months* *Mode of Interview: Phone then F2F* *Descrpition:-* · Bachelor’s degree in life science, statistics,mathematics, computer science, or related field is required; Master’s degree is preferred. · 8 plus years Pharmaceutical/CRO experience as a SAS Programmer supporting clinical trials for regulatory submissions with a Bachelor’s degree; or 5 plus years experience with a MS/MA degree. · Demonstrated proficiency in using SAS to produce derived analysis datasetsand produce TFLs. · Thorough understanding of clinical data structures, relational database structures, and data exchange with alternate data formats. · Demonstrated skills in using additional software tools and applications (e.g. · MS office, XML). · Demonstrated expertise in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM. · Demonstrated expertise in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission. · In-depth understanding of regulatory, industry, and technology standards and requirements. · Good knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs. · Demonstrated ability to work in a team environment with clinical team members. · Good interpersonal, communication, writing and organizational skills. *5 DAYS ON SITE WORK ONLY)* *(EXPERIENCE OF WORKING ON ONCOLOGY STUDIES IN MEDICAL AFFAIR GROUP IS* *PREFERRED:* *Responsibilities will include, but are not limited to, the following:* · Provide programming input to CRF, SAP, analysis file specifications, and tables, figures, and listings (TFLs) shells. · Write SAS programs to generate derived analysis datasets, perform analysis, and TFLs. · Perform ad hoc flexible and rapid programming arising from questions generated from planned analyses and results. · Ensure consistency and adherence to standards within their therapeutic are · Provide programming support for the preparation of integrated reports, submissions and post-submission activities. · Oversee the services provided by CROs. · Contribute to the creation, maintenance, and validation of standards for programming tools, outputs and macros. · Provide training on departmental SOPs/WPs and standard programs. · Contribute to the creation of naming conventions and standards for the programming environment. · Participate in industry wide technical discussions. Regards, *Heera Chaudhary* (Technical Resource Specialist) *Ramy Infotech*--consulting redefined 5201 Great America Parkway Suite 320, Santa Clara, CA 95054 Phone : 408-317-9256 Ext-336 Fax : 408-273-6834 Email : *[email protected] <[email protected]>*URL : www.ramyinfotech.com Gtalk Id: *heera.ramy* YM Id: *[email protected] <[email protected]>*In My Absence, Please Contact Anchal Rastogi | Phone: 408-317-9256|Ext: 335|E-mail: - [email protected] *Disclaimer**: The information in this email is confidential and may be legally privileged. Access to this email by anyone other than the intended addressee is unauthorized. If you are not the intended recipient of this message, any review, disclosure, copying, distribution, retention, or any action taken or omitted to be taken in reliance on it is prohibited and may be unlawful. If you are not interested in receiving mails from us then please forward this mail with "remove" in the subject to [email protected] <[email protected]>. Sorry for any inconvenience* -- You received this message because you are subscribed to the Google Groups "Oracle Developers" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at https://groups.google.com/group/oradev. For more options, visit https://groups.google.com/d/optout.
