*Only C2C* Hi
Hope you are doing well I am Steven, working as a recruiter with Infotree Service Inc. I am currently working on “*Biostatistician”* position with *Eisai, Inc.* I will appreciate your response at the earliest, as the managers tend to move fast! *NOTE :** SEND RESUMES WITH THESE DETAILS , Profiles with all mandatory details would be processed with TOP Priority* *Name (First & Last)* *Contact No.* *Email ID * *Current Location* *Willing to Relocate if need* *Work Visa Status*, *Expiry Date* *Availability * How soon can you join?* *Reason for change* *Are you fine with drug and background check?* *Skype ID* *Last 4 Digit SSN No.* *DOB(Day, Month)* *Higher Education, Year of Completion * *Job Title* *Biostatistician* *Project Location* *Woodcliff Lake, NJ 07677* *Duration* *12 months plus (tenure here is 36 months)* *Summary:* Eisai, Inc. *Biostatistician (Contract)* This is a higher level position Under the guidance of lead project statistician • Work with the *clinical study team* on study design, development and/or review of *clinical study protocols*. • Develop and/or review *statistical analysis plans*, including Table/listing/figure shells, and final study report for clinical studies; • Work with clinical data managers on design/review of case report form, data transfer specification, edit check specification, and participation in user acceptance testing (UAT); generate/review data tables/listings and coordinate data review meetings during the course of the study to ensure data quality. • Oversee programming activities, perform quality assurance checks on internally or externally produced *SAS tables, listings, and figures, and ensure the quality of deliverables*. Perform post-hoc statistical analyses as needed. • May work on submission teams as a statistician and/or a programmer. • Generate and *QC outputs* for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies • May serve as lead Statistician on complex trials and across multiple studies. *QUALIFICATIONS NEEDED: * • Must have a *MS in* *Biostatistics/Statistics* with at least 5 years of experience or a PhD in Biostatistics/ Statistics with at least 3 years of experience in the pharmaceutical, CRO or biotech industry. • Strong *SAS programming* skills. – at least 3-5 years. • *Oncology *experience is highly preferred. • Good communication skills (verbal and written). • Ability to effectively work on *multiple projects* *Thanks & Regards,* *Steven* - Technical Recruiter *Phone *(Direct): 734-888-8174 *Email:* ste...@infotreeservice.com <st...@infotreeservice.com> | *Website:* www.infotreeservice.com *LinkedIn:* https://www.linkedin.com/pub/steven-fernandez/104/956/240 *Hangout:* steven.usrecruiter | *Yahoo:* steven.usrecruiter *Mailing Address:* 215 Ann Arbor Rd. Suite 304 Plymouth, MI 48170 [image: Description: Description: Description: cid:image001.jpg@01D047B2.F3DC0D60] ------------------------------ “This message and any attachments are solely for the intended recipient and may contain confidential or privileged information. If you are not the intended recipient, any disclosure, copying, use, or distribution of the information included in this message and any attachments is prohibited. If you have received this communication in error, please notify us by reply e-mail and immediately and permanently delete this message and any attachments. Thank you.” -- 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 http://groups.google.com/group/oracle-projects. For more options, visit https://groups.google.com/d/optout.
