Hi, We have potential openings for the following skills with one of our client. Please let us know your interest by sending a copy of your resume in MS Word format.
Please only submit resumes along with below details in order to proceed further: Full Name: Current Location: Relocation: Legal Status: Availability to start: Availability for Webcam Interview: Contact: Email: Skype ID for webcam interview: Rate: Couple of References: Reference:1 Name : Designation : Email ID: Contact : Reference:2 Name : Designation : Email ID: Contact : *Matrix:* Skill Years Of Exp Overall Industry Exp Statistical CDISC SDTM/ADaM datasets QC/Validation of SAS code Macro, GRAPH SR SAS Programmer Location: South SFO, CA Duration: 6+ Months 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. -- Thanks and Regards, BenLee Sr. Recruiter Vectorsoft | Email: <b...@vectorsoft.com>b...@vectorsoft.com | -- You received this message because you are subscribed to the Google Groups "Oracle-Projects" group. To unsubscribe from this group and stop receiving emails from it, send an email to oracle-projects+unsubscr...@googlegroups.com. To post to this group, send email to oracle-projects@googlegroups.com. Visit this group at https://groups.google.com/group/oracle-projects. For more options, visit https://groups.google.com/d/optout.
