Theorem Clinical Research currently has multiple openings for permanent Programmer positions that can be done remotely anywhere in the US. At the moment we need to hire 2 SAS Programmer Analysts, 5 Sr. SAS Programmers, and 2 Lead SAS Programmers, with more project awards on the way soon.

For programmers: Bachelors in minimum, masters is preferred.

A little more info about programmer position Job Title: Programmer Analyst
Department: Biometrics BB01
Country: U.S.
Requirements: TRAINING & EXPERIENCE 4 year computer science/math degree or equivalent; MS preferred 2-4 year’s clinical programming or SAS programming experience 1-2 years’ experience using SAS Major part of work done in office environment. Proficient in at least one computer language, i.e., PASCAL, FORTRAN.

KEY SKILLS & BEHAVIORS Communication/relationships with othersWork extensively with Biometrics project team membersInteract with members of Company project team
Job Description: SUMMARRY
SAS programmer who should be able to produce basic analysis displays and information from the clinical data management database

RESPONSIBILITIES
All responsibilities from the Programmer position will be performed, in addition to the following: Handle tasks as assigned by managementCreate SAS datasets of clinical data from clinical databases; create status and efficacy datasets; create project specific macros and formats; load client data from other platforms and other software packages; prepare data to be sent to clientsPrepare documentation describing all datasets and variables within, including derived variables, and the project as a wholePerform data checks as needed, to ensure integrity and correctness of data displays. Prepare documentation for programsProgram customized data displays, (including data listings, summary tables and routine graphics) in accordance with approved statistical analysis plan and shell displays for clinical research studies. Code is to be written using Base SAS programs, SAS procedures, or standardized macros. Perform data checks as needed to understand structure and content of data.Act as lead programmer for projects

  For statisticians: Masters or PhD… A little more info about stat position
Job Title: Statistician II
Department: Biometrics BB01
Country: U.S.
Requirements: TRAINING & EXPERIENCE M.S./Ph.D. in Statistics/Biostatistics or equivalent discipline 1−3 years experience in the analysis of clinical data for M.S. 0−2 years experience in the analysis of clinical data for Ph.D No special physical demands Some travel required for meetings Major part of work done in office environment Proficient in SAS
KEY SKILLS & BEHAVIORS Work extensively with Biometrics project team members.Interact with other members of Company project team.Respond to questions from clients.Effectively communicate data findings to the data manager and results to Company clinician, project manager, and sponsor staistician.
Job Description: SUMMARY
Statistician who should be able or is learning to perform all basic analysis and is gaining exposure to more complex analysis for a clinical
trial.

RESPONSIBILITIES Conduct basic and assist with complex statistical analysis in support of clinical research studies as specified in statistical analysis plans, including statistical graphics. Verify randomization codes for a basic study design and develop randomization specifications for basic and complex study designs. Prepare statistical sections of protocols (including sample size determinations)and statistical analysis plans. Prepare and annotate safety and basic and complex efficacy shell data displays. Provide specifications for structure, content and algorithms for safety and efficacy analysis datasets. Perform and quality control of data displays that show basic and complex inferential statistics. Perform quality control of safety and efficacy analysis datasets. Maintain project administration file, including protocol, annotated CRF, statistical analysis plan, annotated shells for data displays, programming and quality control rules, tracking of generation and quality control of data displays, and project communication (internal and client). Maintain project directories on computer systems, including ensuring that final SAS output is in the correct directory, and that all interim programs and output are deleted at the completion of the project. Handle miscellaneous tasks as assigned by management. Able to review case report (CRF)design, data management plan, and edit specifications for a clinical trial. Able to review clinical study report (CSR)for statistical concerns. Able to provide input to standard operating procedures (SOP)and audits. Able to mentor new hire statisticians. Able to propose solutions to problems that arise while performing tasks. Perform quality control of datasets and data displays for integrated summary of safety and efficacy. Produce quality deliverable within timelines and with customer satisfaction. Develop effective time management skills.
  Ronnie DeFrancis
Senior Programmer/Analyst, Biometrics
Theorem Clinical Research
Phone: (919) 782-0941
www.theoremclinical.com