Statistician/Statistical Programmer

Details: We have looking for Biostatistician/Statistician/Statistical Programmer with a stable work history and very strong communication skills for a leading Pharmaceutical product and development Companies located in Wayne, PA and RTP, NC area. Biostatistician/Statistician will provide statistical support for clinical/non-clinical development projects and programs. Market Rate, c ommensurate with education and work experience. Multiple openings, one year (renewable) contract, contract-to-perm. ***Available for H1B/EAD/U.S. Citizen/Permanent Resident based on W2 or Corp-to-Corp/1099. Please forward your resume to or call Rose Chu at 610-822-1256 for questions. ***These opportunities require Master degree in Statistics, Biostatistics and EXCELLENT communication skills*** Please only apply when English is the your native language with M.S./Ph.D. in Statistics or Biostatistics Notes: required * 4-5 years pharmaceutical industry Statistical Programming or Statistical Analysis (Statistician) experience with Masters degree in statistics* ; * 2-3 years pharmaceutical industry Statistical programming or Statistician experience if you have Ph.D. in statistics or biostatistics* and would not mind to assist in QC SAS coding/etc. If you are interested in aligning with a highly regarded organization that values quality and integrity and fosters an environment where teamwork and professionalism thrive, then don’t hesitate to contact us by submitting your resume for future opportunity or call Rose Chu, VP in Pharmaceutical & Biotech Services Group at #610-822-1256 for questions. We are always interested in talking to candidates for current AND future opportunities! Please respond directly to Global Employment Solutions, Inc. with your resume attached –WORD document. SUMMARY: This person will be responsible for statistical contributions to Clinical Study reports, programming of efficacy tables, and statistical analysis. A person in this position will work with SAS programs to analyze and summarize the data, SAS graphs and validation of statistical analyses and findings. Assist in SAS coding/etc. RESPONSIBILITIES: • Provides input and review on design of studies, protocols, and case report form (CRF) design; • Computes sample sizes in conjunction with clinical staff as required for clinical studies; • Writes detailed analysis plans and analyzes clinical data, as directed by immediate supervisor; • Designs or oversees the design of summary tables, reports, and graphs for presentation of results; • Designs data surveillance plans and analyzes results for trends; • Writes statistical analysis descriptions for protocols and final reports, as directed by immediate supervisor; • Consults with others in company on statistical issues when requested; • Creates and modifies, or directs the creation and modification of, SAS programs to support all of the above; • Checks and verifies statistical programs, data listings, and summary tables; • Maintains statistical and programming activities and documentation in accordance with Company’s policies, procedures and all standard operating procedures (SOPs); Keywords: Statistician, Biostatistician, Clinical Statistician, Statistical Analysis, SAP, Ph.D. Statistics, Ph.D. Biostatistics, Master Statistics, MS Statistics, MS Biostatistics, SAP, SAS, Lead Project Statisticians, biostatistical components, statistical component. Applies statistical, Applied Statistics, Statistical Programming, Biostat, Stat , Statistical Consultant, Statistical Programmer Knowledge, Skills, and Competencies • Masters or PhD in biostatistics or statistics is required. • 2 to 5 years of pharmaceutical industry statistical programming or statistician experience with Masters or Ph.D. in Statistics or Biostatistics • Substantial knowledge of SAS System programming required; • Minimum of one years experience using SAS required ; • Familiarity with statistical methods used for biomedical/pharmaceutical research required; • Experience with clinical trials or pharmaceutical industry experience required; • Knowledge of current industry and regulatory submission practices, protocol designs, and terminology. We appreciate your understanding, in that; we will only be able to respond to those inquiries who meet the stated requirements. To protect our client’s interests, we will not be responding to inquiries that do not contain a CV/Resume. Finally, please include the position ID (rc- Statistical Consultant ) in the subject line of your correspondence to ensure review. Please forward your credentials in Word format to in confidence, to: Rose Chu through Indeed Rose Chu Vice President Pharmaceutical, CRO, Biotech, Medical Device Global Employment Solutions, Inc. 610.822.1256 phone Referral Bonus Program – $250 + IPad: Please call for details

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