Joulé Inc.
One Company… Many Specialties…Your Best Choice!


Joule Joulé's Goal: To create a first experience that will convince you that Joulé is your "best" choice. And then to repeatedly create positive experiences for you!

Joulé is currently looking for


Title of position: Database Programmer I
Job location: King of Prussia, PA
Number of openings: 1 /temporary to permanent
Contact Person: Matthew Pepe @800-810-5587 x302 or email mpepe@jouleinc.com

Requirements:

  • University/College degree or relevant experience
  • 1-2 years using SQL/SAS or 1-2 years industry experience programming
  • Experience with Oracle Clinical a plus!
Job Description:
    Provide programming or other support and assist CDM managers in daily technical operations. Respond to and solve technical oriented problems in a timely manner, as appropriate for the position.
  • Develop project specific procedures for loading external data and/or transferring internal data and verifying the process. Ensure client specifications for data transfers are met and be responsible for receiving or sending internal & external data.
  • Develop procedures for loading client dictionaries and verifying the process, as appropriate for position. Ensure client specifications for dictionary loading is addressed.
  • Ensure client specifications for coded data transfers are met and be responsible for receiving or sending internal & external data.
  • Provide programming or other support and assist CDM managers in daily technical operations. Respond to and solve technical oriented problems in a timely manner, as appropriate for the position. Assist data manager with status reports and listings as necessary
  • Interact with Biometrics and other departments concerning database contents and structure as necessary.

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Title of position: Sr. Programmer Analyst (SAS)
Job location: King of Prussia
Number of openings: 1 /temporary to permanent
Contact Person: Matthew Pepe @800-810-5587 x302 or mpepe@jouleinc.com Requirements:

  • 4 year computer science/math degree or equivalent; MS preferred.
  • 1-2 year's clinical programming or SAS programming experience.
  • Proficient in at least one computer language, i.e., PASCAL, FORTRAN.
  • High degree of accuracy and attention to detail.
Job Description:
  • Act as lead programmer for projects.
  • Program 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.
  • Perform data checks as needed, to ensure integrity and correctness of data displays. Prepare documentation for programs.
  • Prepare documentation describing all datasets and variables within, including derived variables, and the project as a whole.
  • Create 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 clients.
  • Handle miscellaneous tasks as assigned by management.

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Title of position: Clinical Programming Specialist
Job location: Exton, PA
Number of openings: 1 /direct hire
Contact person: Matthew Pepe @800-810-5587 x302 or mpepe@jouleinc.com

Requirements:

  • BS Mathematics, Statistics or similar
  • 4 years of clinical programming experience
  • Strong knowledge of clinical programming principles
  • Demonstrated ability with SAS
  • Ability to effectively direct others
  • Should not require instructions on routine assignments and only require general instructions on new assignments

Job Description:

  • Follows established standards and procedures to provide a wide range of clinical programming duties involving designing, developing, evaluating, and modifying SAS programs to analyze and evaluate clinical data
  • Load SAS datasets, containing clinical data from external sources, into Company’s SAS system for clinical trial data
  • Verify SAS datasets, containing clinical data from external sources, with Company dataset standards
  • Develop mock tables for clinical study reports from a library of standard mock tables
  • Write/edit and execute SAS programs that produce derived datasets
  • Write/edit and execute SAS programs that produce moderately complex clinical data summaries, figures and listings
  • May provide direction to other clinical programming employees
  • Comply with Company SOPs and departmental guidelines and procedures
  • Other activities as required by management
  • No travel required

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