Hello,
Please go through the below requirement and let me know on [email protected]. If you have any suitable candidate please share with me your candidate resume. Job Title : Sr. SAS Programmer Location : Los Angeles, CA or Sun Francesco, CA Duration : 6 Months + Option for Extension Interview Mode : Phone / Skype Job Description Overview: Our Biotechnology client needs to hire a Senior SAS Programmer for a long term contract based in Los Angeles OR San Francisco. They have experienced tremendous success with its oncology drugs in clinical trials and is ready to integrate resources with a clinical SAS programming background into the company. Reporting to the Sr. Director of Statistical Programming, the Sr. SAS programmer, Statistical Programming, will gather and analyze user requirements, program complex deliverables, work closely with study team and deliver consistent high quality results on time. Responsibilities: · Create SAS programs for data mining · Gather study team requirements and translate them into technical specifications for SAS programs · Program SAS data validation checks and listings to identify data discrepancies · Program SAS checks to integrate and reconcile data from external sources including serious adverse events (SAE), lab results, ECGs, electronic patient records, medical devices and interactive voice response (IVR)] into the primary clinical database SAS datasets · Review Case Report Forms and formatting of SAS datasets extracts for accuracy and consistency · Provide programming support for Annual Safety Reports and Publications · Build standard SAS Macro library · Mentor junior level SAS programmers, if needed · Provide Ad hoc statistical programming support Skills Required: · Bachelor's Degree in related area · Minimum of 7 years of SAS programming experience in the biotechnology/pharmaceutical industry · Excellent SAS 9.3 programming skills · Solid knowledge of CDISC/ Study Data Tabulation Model (SDTM), ICH/GCP, 21 CFR 11 · SAS 9.3 (Datastep, Procedures, Macro, Proc SQL etc.) · Knowledge of Oncology clinical trials · Familiarity with Data Management software (e.g. Medidata, Oracle Clinical) · Familiarity with coding dictionaries - MeDDRA and WHODRUG Years’ Experience Minimum of 7 years Darshan Patel | Sr. Recruiter | T: 218-656-0390 | email id: [email protected]| Gmail id: [email protected] Rider Consulting Inc | 50 Cragwood rd, suite 205, South plainfield, New jersey | www.riderconsultinginc.com -- You received this message because you are subscribed to the Google Groups "US_IT.Groups" 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/us_itgroups. For more options, visit https://groups.google.com/d/optout.
