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Sr. Statistical Programmer
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Country: USA
Location: Massachusetts-Boston Cambridge, MA 02139
Total applied: 40 Job Category:Biotech/R&D/Science
Location:Cambridge, MA 02139
Status:Full Time, Employee
Occupations:Mathematical/Statistical Research;General/Other: R&D/Science
Career Level:Experienced (Non-Manager)
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Sr. Statistical Programmer
Description:
The Sr Statistical Programmer will develop and design SAS computer programs that access, analyze and report clinical trials data , in accordance with SAP, ICH guidelines, and applicable regulatory requirements. Individual will be responsible for the development, maintenance, and production of data listings, summary, validation and analysis programs that meet specifications described in trial documentations. The incumbent will have the following responsibilities:
Be responsible for the development, maintenance, and production of TLFs;Use, modify and maintain existing SAS program code as necessary;Assist in the preparation of the regulatory submission-ready packages;Conduct programming and documentation for regulatory submissions; Follow good programming practices and adequately document programs; Create and maintain file structures for storing clinical data;Assist in reviewing DMP, CRF design and other CDM documents;Assist in reviewing SAP and other related documents;Other duties as assigned. Requirements:
Bachelor's degree in Math, Statistics, Computer Science or other related field with five years SAS programming experience or equivalent; or Master's degree in Math, Statistics, Computer Science with 3 years in industry related (Pharmaceutical, Biotech, CRO) SAS programming experience or equivalent;Knowledge of clinical trials and experience in using SAS to report the results of clinical trials;Experience in constructing technical programming specifications and producing validated SAS programs;Excellent knowledge of SAS Macro, SAS/SQL, SAS/GRAPH and SAS/STAT;Excellent knowledge of DM processes;Comprehension of CDISC requirements;Knowledge of clinical trial development process;Familiar with medical coding dictionaries (WHO-DRUG ®, MedDRA™ );Excellent written, verbal and interpersonal communication skills;Strong organizational and analytical skills.
AVEO is a clinical stage private biopharmaceutical company focused on the discovery and development of novel, targeted cancer therapeutics. AVEO’s proprietary, integrated cancer biology platform enables the company to pursue highly efficient drug development strategies in oncology that increase the probability of clinical success and provides a discovery engine for high-value targets. This approach has resulted in a balanced pipeline of novel cancer therapies focused on well-validated targets (VEGFR, EGFR) and promising novel targets (HGF), as well as collaborations with Merck, OSI Pharmaceuticals and Schering-Plough. Through a combination of internal drug discovery and selective in-licensing of targeted therapeutics, AVEO is building a diversified product pipeline and moving toward its vision of becoming a fully integrated biopharmaceutical company. For more information or to apply to this position, please visit the company's website at www.aveopharma.com.
Please forward resumes to hr@aveopharma.com .
AVEO is an Equal Employment Opportunity employer that values the strength diversity brings to the workplace.
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