Senior Principal Statistical Programmer Top BioPharma

RBW Consulting Solutions Ltd
$Exceptional salary + very strong and benefits pac
18 Apr 2017
27 Apr 2017
A Global Biopharma with offices in Boston Massachusetts looks to add a senior tier Statistical Programmer to its growing team. Role - Function as the Lead for multiple global clinical studies, across one, or more than one clinical development programmes - Be an expert in regulatory requirements (SDTM & ADaM standards, etc.) - Lead the programming portion of regulatory submissions - Oversee, direct and quality check the work of CROs, in line with project needs - Functionally manage and mentor junior Programmers - Offer skills and expertise to other project groups in a consulting fashion Required - 6 years relevant experience in a Pharma, Biotech or CRO - Minimum of a Bachelors in a relevant subject - Exceptional working knowledge of CDISC (both SDTM and ADaM) - Demonstrable experience in a position of leadership (study, project or programme) - Good knowledge of the regulatory submissions process - Advanced proficiency in SAS - Strong communication skills I manage a range of other permanent and freelance positions for a broad portfolio of clients (Biotech, CRO and Pharma). If the above role isn't for you but you'd nevertheless like to discuss your options in the market, I'd welcome a confidential discussion by phone or email. Contact Daniel Cheetham at (617 982 1238. Keywords SAS, SAS Programmer, Project Lead, Statistical Programmer, Stat Programmer, Clinical Programmer, Data Programmer, Database Programmer, Statistical Programmer I, Statistical Programmer II, Senior Statistical Programmer I, SAS Programmer I, SAS Programmer II, SAS Programmer III, Senior SAS Programmer I, Senior SAS Programmer II, CDISC, SDTM, ADaM, ADAM, Junior Programmer, Graduate Programmer, Project Lead Programmer, Lead Programmer, Manager of Programming, Senior Manager of Programming, Director of Programming, Statistical Programmer, SAS Programmer