*Hi**,*
*Hope you are doing great!!*
* Please find the requirement below **,* *If you find yourself comfortable
with the requirement please reply back with your updated resume with
details to this email id s.dak...@esskay-inc.com <s.dak...@esskay-inc.com>
and I will get back as soon as possible.*
*Position: SAS **Programmer Analyst*
*Location:* * South Mounds View, MN*
*Project Duration: 12+ months*
*Job Description:*
This is a statistical programmer/analyst position, programming in SAS every
day. Tasks may include production and validation programming for clinical
reports (e.g., tables, listings, and graphs), creating SAS datasets and SAS
analysis datasets (can merge from multiple sources and create derived
variables), ad-hoc listing (e.g., to help with data cleaning), and creating
study management reports (e.g., data quality report). Work will be done
according to standard operating procedures for development and
documentation of work. Industry experience is a must. (Pharma, research
institutes, clinical, medical facilities) This is not a data management
role. It is more analysis and reporting centered. Candidates must possess
leadership abilities, work within a team environment and be open to other
duties as they are assigned.
*Responsibilities: *
- Plans and coordinates programming, testing, and documentation of
statistical programs for use in creating statistical tables, graphics, and
listing summaries.
- Programs analysis database manipulations and transfers of data for
internal and external clients.
- May integrate databases from multiple studies or sources.
- Develops listing and table specifications with study Biostatistician.
- Interact with Data Management and Biostatistics staff and SP team
members to negotiate timelines, responsibilities, and deliverables.
- Understands and complies with Standard Operating Procedures and Work
Instructions.
- Programs, tests, and documents statistical programs and tools in
accordance with SP standards and validation procedures.
- Meets milestones as assigned.
- Performs other duties as directed by Statistical Programming
management. Will be working on CRDM trials.
- Experience using *SAS for more than 2 years and using SAS on
clinical trial data analysis*.
- Industrial experience is preferred
- Regulatory submission experience is a plus
- Prefer the candidate has industry experience and had experience with
PMA submission etc.
- Absolute skill is SAS programming skills including *SAS
BASE/STAT/MACRO/SQL etc*.
*Notes:* Hiring manager prefers candidates that are able to potentially get
hired on full time. Local candidates preferred. Position may potentially be
extended up to 2 years total.
*Required Skills:*
Education Level: High School Diploma or Equivalent
Program Languages: *SAS*
Software Application Knowledge: *SAS*
MS Excel
*Program Languages: *SQL
Unix Shell Script
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