• Clinical Research Developer

    Job Locations US-NC-Cary
    Requisition ID
    Research and Development
    Visa Sponsorship
    Travel Requirements
  • Overview

    Germany SAS


    JMP is an independent R&D division of SAS with a 25 year history of providing interactive, graphical, statistical discovery software to the engineering and scientific communities.  The JMP Family of Products includes JMP Clinical and JMP Genomics, two solutions integrating JMP and SAS that are dedicated to vertical applications in life sciences research. 


    We are seeking a highly motivated Clinical Research Developer who will be responsible for developing and supporting JMP Clinical reports for clinical trial safety, efficacy, and data site integrity analysis.  JMP Clinical integrates SAS programming and JMP interactive visualization to create analysis reviews for biometrics, medical monitors and writers, regulatory reviewers and clinical data management and operations user roles.  The solution leverages CDISC standard data models (SEND, SDTM and ADaM) and knowledge and experience programming around these domain structures is a must.


    Essential Requirements:

    • MS or PhD in Biostatistics/Statistics, Computer Science, life/analytical sciences or related field.
    • 5+ years’ experience in SAS programming (SAS/BASE, STAT, and Macros) for phase I-IV clinical trials research
    • Significant knowledge of drug development and clinical trial processes with experience working with cross-functional teams
    • Demonstrated understanding of CDISC requirements and implementation guidelines for regulatory submissions
    • Strong familiarity with GCP, ICH, and FDA guidelines and regulations applicable to conduct clinical research.
    • Ability to perform multiple tasks efficiently and accurately with minimal supervision while meeting deadlines.
    • Ability to learn new programming languages, technology, tools and processes.
    • Strong written, verbal, interpersonal communication skills to work effectively in a collaborative team environment


    • Experience with JMP, JMP Clinical or similar products
    • Experience with JMP Scripting Language (JSL), R, Python or other scripting languages
    • Experience with data visualization concepts and user interface considerations
    • Demonstrated leadership in clinical trial programming and support of therapeutic areas (oncology preferred)
    • 3+ years CDISC experience


    SAS looks not only for the right skills, but also for a cultural fit. We seek colleagues who will contribute to the unique culture that makes SAS such a great place to work. We look for the total candidate: technical skills, culture fit, relationship skills, problem solvers, good communicators and, of course, innovators. Candidates must be ready to make an impact.


    Additional Information:

    To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.SAS is an equal opportunity employer.  All qualified  applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law. The level of this position will be determined based on the applicant's education, skills and experience. Resumes may be considered in the order they are received. SAS employees performing certain job functions may require access to technology or software subject to export or import regulations. To comply with these regulations, SAS may obtain nationality or citizenship information from applicants for employment. SAS collects this information solely for trade law compliance purposes and does not use it to discriminate unfairly in the hiring process.


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