PAREXEL International LLC Associate Director, Software Engineering in Billerica, Massachusetts
Associate Director, Software Engineering
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Job ID82707BR Billerica, Massachusetts
Duties: Parexel International LLC seeks an Associate Director, Software Engineering in Billerica, MA, working under minimal supervision, design and develop ETL mappings and workflows using Informatica Power Center 9.x and B2B DX and DT technologies in FDA/21 CFR Part 11 and GxP regulated clinical trials domain. Develop technical specifications for data loading rules. Design, implement and architect software products and extensions for customer specific requirements. Produce technical specifications, data models, installation and qualification guides, and release notes for software development processes. Design logical/physical database structures and develop entity-relationship diagrams. Perform data modeling. Design and support clinical trials information sharing solutions. Design and implement large scale ETL solutions managing big data. Design and implement data warehouse, multi-tier applications, web services, data-driven systems with large-scale relational or object-oriented databases. Implement PL-SQL and Oracle 11.x. Apply 4GL programming skills, particularly UNIX shell and Perl scripting languages. Perform informational modeling techniques, applying Kimball's dimensional modeling techniques. Utilize technical information standards XML, XSL, and XSLT transformation technologies. Utilize configuration management tools SVN and CVS to execute live deployments. Provide developing solutions for pharmaceutical/clinical trials domain. Develop clinical data collectors - CTMS, EDC, RTSM, and safety systems. Perform Agile software development methodology. Apply clinical information standards CDISC, SDTM, ODM, HL7, and BRIDG. Position may work from home 2-3 days per week. Qualifications Requirements:Master's degree in Computer Science, Computer Engineering, Electronic Engineering, or a related field plus one year (or Bachelor's degree plus 5 progressive years) of software development experience in:
FDA/21 CFR Part 11 and GxP regulated clinical trial domain;
ETL design, development, architecting and data warehousing experience;
Database development experience with PL-SQL, Oracle 11.x, 4GL programming, UNIX shell, and Perl scripting languages;
Informatica PowerCenter 9.x and B2B DX and DT technologies; and
Agile development software methodology.
Must have at least one year of experience with SGL Automation, Toad, Tortoise SVN, Data Modeler and Analysis, XML XSL, XSLT, and AJAX technologies.
Will accept any suitable combination of education, training or experience.
To apply, please send resume to email@example.com and cite requisition number 00518, or apply at jobs.parexel.com, or click the apply button. This notice is subject to Parexel International LLC's employee referral program.
EEO DisclaimerParexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.