Hello Partners, Find the details of the requirements as below and send me the matching profiles to ku...@absli.com
*Start Date*: ASAP Location: NJ Duration: 6 Months Plus *Senior Statistical Analyst** (6 positions):* *Job Duties:* · Review protocol, CRFs, and statistical analysis plans · Develop SAS programs for the analysis and reporting of clinical trials · Validate analysis datasets and SAS programs written by other programmers · Ensure development of programs according to project standards · Integrated analysis of clinical studies · Creation of the database and programs package for submission to regulatory authorities · Contribute to project standards development · Comprehensive overview of project development details and data history · Participate in study team meetings and teleconferences · Work in close collaboration with biostatisticians and data management, and directly communicate with sponsor’s study team and managers *Requirements:* · Bachelors degree in Computer Science, Biostatistics, Mathematics, or equivalent · At least 3 years relevant experience in the pharmaceutical/ biotechnology industry · Experience of SAS/MACRO, SQL, SAS/BASE, SAS/GRAPH and Statistical procedures · Understanding of the concepts of descriptive statistics for numerical and categorical data and ability to implement SAS to generate summary statistics · Experience of MedDRA and WHODD dictionaries · Experience of preparing IND/NDAs for regulatory agencies · Experience of PK/PD Programming · Capable of clear and timely written/verbal communication with statisticians and study team · Some knowledge and experience with CDISC desirable ____________________________________________________________________________________________________________________________________ *Lead Statistical Analyst** (2 positions):* *Job Duties*: · Review protocol, CRFs, and statistical analysis plans · Develop SAS programs for the analysis and reporting of clinical trials · Validate analysis datasets and SAS programs written by other programmers · Ensure development of programs according to project standards · Integrated analysis of clinical studies · Creation of the database and programs package for submission to regulatory authorities · Contribute to project standards development · Comprehensive overview of project development details and data history · Participate in study team meetings and teleconferences · Work in close collaboration with biostatisticians and data management, and directly communicate with sponsor’s study team and managers · Leads will oversee completion of programming and validation of analysis datasets, tables, listings and figures for assigned studies and projects · Leads will work independently with minimum oversight · Leads will coordinate activities of assigned team members · Leads to provide technical mentorship to junior programmers · Understand timelines for and milestones affecting their work and alert supervisor to potential slippage *Requirements*: · Bachelors degree in Computer Science, Biostatistics, Mathematics, or equivalent · At least *5 years relevant experience in the pharmaceutical/ biotechnology industry* · Experience of *SAS/MACRO, SQL, SAS/BASE, SAS/GRAPH and Statistical procedures** *· Understanding of the concepts of descriptive statistics for numerical and categorical data and ability to implement SAS to generate summary statistics · Experience of MedDRA and WHODD dictionaries · Experience preparing IND/NDAs for regulatory agencies · Experience of PK/PD Programming · Capable of clear and timely written/verbal communication with statisticians and study team · Knowledge and experience with CDISC desirable · Leads should be able to draft programming specifications according to SAP · Leads should have experience of leading programming teams and projects -- Regards Alrek Business Solutions, Inc. (Formerly Known as ALDON BUSINESS SOLUTIONS, INC) 830 E.Higgins Rd, Suite # 114, Schaumburg, IL 60173 URL:www.absli.com Ph: 847-348 0380, 1194 Fax: 847-4138294 Certified Minority Business Enterprise(MBE) CONFIDENTIALITY NOTICE: This e-mail message including attachments, if any, is intended only for the person or entity to which it is addressed and may contain confidential and /or privileged material. Any unauthorized review, use, disclosure or distribution is prohibited. If you are not the intended recipient, please contact the sender by reply e-mail and destroy all copies of the original message. If you are the intended recipient but do not wish to receive communications through this medium, please so advise the sender immediately -- You received this message because you are subscribed to the Google Groups "Open Source Erp & Crm" group. To post to this group, send email to open-source-erp-...@googlegroups.com. To unsubscribe from this group, send email to open-source-erp-crm+unsubscr...@googlegroups.com. For more options, visit this group at http://groups.google.com/group/open-source-erp-crm?hl=en.
