Clinical SAS Programmer
Job ID : 33195
Job Title : Clinical SAS Programmer
Location : Princeton NJ
Comapny Name : Merit Technology Services
Job Type : Full-Time, contract
Industry : Healthcare
Salary : $35000 - $60000 per year
Work Authorization : ["OPT","CPT","F1"]
No. of Positions : 10+
Posted on : 12-14-2022
Required Skills : SAS/BASE, SAS/STAT, CDISC,
Benefits : Medical Insurance
Job Description :
Responsibilities:
· Responsible for coordinating and programming of clinical data analyses.
· Analyzes and evaluates clinical data, recognizes inconsistencies and initiates resolution of data problems.
· Typically programs using SAS language to support the clinical area.
· Implements statistical analysis plans.
· May consult in the design and development of clinical trials, protocols, and case report forms.
· Validate work of other programmer(s)
· Ensure the maintenance of programming documentation (e.g. description of programs and validation)
· Interacts with statisticians, data management personnel, project leaders, and sponsors.
· Communicate to management on project status and resource issues
· Investigate and propose initiatives for improving efficiency
· May also serve as Project Leaders on project teams.
· Contribute and take part in client evaluations, visits and bid defenses
Qualifications:
· Requires a Bachelor’s degree, Master’s degree preferred in a scientific discipline
· SAS Advance Programming Certificate preferred
· Thorough knowledge of computer systems, applications and operating systems
· Strong analytical skills
· Ability to simplify complex issues into understandable concepts
· Provide mentoring to junior staff
Skills:
· Strong written and verbal communication skills including good command of English language
· Proficiency with various computer applications such as Word, Excel, and PowerPoint required
· Requires expert knowledge/experience of SAS/Base, especially macros, arrays, formats and ODS.
· Expert knowledge of SAS/STAT and SAS/GRAPH is also required.
· Requires familiarity with basic statistical principles to interact with biostatisticians.
· Requires excellent written skills and ability to interpret and implement table manuals and statistical analysis plans.
· Requires advanced knowledge of drug development principles related to the production of databases and summary tables, such as CDISC standards.
· Requires ability to write validation plans.
Company Details :
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