Clinical Programmer

1 week ago

Bridgewater, New Jersey, United States Meet Life Sciences Full time

Overview

We are seeking a
Senior Statistical Programmer
to provide programming support for clinical studies and regulatory submissions. This role involves developing, validating, and maintaining CDISC-compliant datasets and outputs to support data analysis and reporting activities.

Key Responsibilities

  • Develop and validate
    CDISC-compliant SDTM and ADaM datasets
    in support of clinical studies and submissions.
  • Create and maintain programs to generate
    tables, figures, and listings
    (TFLs) for ad-hoc analyses and publications.
  • Draft and maintain
    dataset specifications
    in accordance with SDTM IG, ADaM IG, and SAP.
  • Develop and optimize
    SAS macros and utility programs
    to streamline processes.
  • Design, test, and implement programming solutions to meet complex project needs.
  • Collaborate effectively with cross-functional teams while managing multiple projects and deadlines.

Qualifications

  • Bachelor's degree in
    Mathematics, Statistics, Computer Science
    , or a related field.
  • Advanced SAS programming skills
    required.
  • CDISC SDTM/ADaM
    experience required;
    submission experience
    strongly preferred.
  • Strong verbal and written communication skills.
  • Experience with additional statistical software (e.g.,
    R, S-Plus, WinBUGS
    ) a plus.
  • Programming experience with
    VBA, C++, or Python
    beneficial.
  • Previous experience in
    pharmaceutical or biotechnology
    industry preferred.

Why Apply

This is an excellent opportunity to leverage your programming expertise in a collaborative, data-driven environment. If you're ready to contribute to impactful clinical research projects, we'd love to hear from you.

Apply today to learn more

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