Job Description :
Location:-NC(REMOTE)
Duration:-6+Months
Interview:-Phone/Skype

Big plus to people with Project Lead experience,


What are the three most important qualifications
1. CDISC experience (SDTM & ADaM) 2. Oncology experience 3. Prior knowledge of CDARS system


SUMMARY:
The Sr. Statistical Programmer will provide experienced technical expertise as part of the Statistical Programming team to meet internal and external clients'' needs. Plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical analysis needs. Provide technical expertise and leadership to theteam. Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.


MAJOR DUTIES AND RESPONSIBILITIES:
Program, plan and co-ordinate the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables and listing summaries, (ii) the programming of analysis databases (derived data sets) and transfers of data for internal and external clients and (iii) the programming of database quality control checks.
Program and plan the integration of databases from multiple studies or sources.
Develop, plan, and co-ordinate programming documentation including plans and specifications, as appropriate, for complex studies.
Perform, plan and co-ordinate the development, implementation and validation of new process technologies, macros and applications.
Fulfill project responsibilities at the level of lead for single complex studies or group of studies.
Provide training/guidance to lower level staff.


MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Masters degree or educational equivalent in computer science or related field and 3 years relevant experience; Bachelor''s degree or educational equivalent in computer science or related field and 5 years relevant experience; or equivalent combination of education, training and experience.


REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Senior level
Lead experience
SDTM and ADaM experience strongly preferred
Previous experience in Pfizer CDARS reporting system a definite plus
Knowledge of statistics and/or clinical drug development process.
Knowledge of electronic submissions (including: knowledge of data submission structures and requirements; experience in creating relevant hyperlinks, etc
Advanced knowledge of statistical computing applications such as Base SAS, SAS/STAT and SAS Macro Language.
Good organizational, interpersonal, leadership, communication skills and multi-tasking abilities.



Thanks and Regards
Varsha Singh
Gemini Consulting & Services LLC