IQVIA is seeking a Technical Designer to lead study build and design activities, and manage updates to specifications and eCRF configurations. You will work with DTL, programmers, validation teams, vendors, statisticians, and client representatives to ensure timely, accurate study delivery.
The role involves developing CDMS specifications aligned with SDTM/CDASH standards, creating Edit Specifications, and contributing to risk management and process improvements across multiple projects.
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Senior Clinical Data Designer: eCRF & EDC Expert employer: IQVIA LLC
At IQVIA, we pride ourselves on being an exceptional employer, particularly for those in the field of Pharmaceutical Development. Our Cambridge location fosters a collaborative and innovative work culture, where you will have the opportunity to influence scientific direction, mentor junior scientists, and engage directly with clients. With a strong focus on employee growth and the integration of cutting-edge AI-enabled approaches, we are committed to supporting your professional development while making a meaningful impact in the pharmaceutical industry.
