Clinical Study Report Developer

6 days ago


Reading, Reading, United Kingdom IQVIA, Inc. Full time

Job Overview

IQVIA, Inc. is seeking a highly skilled SAS Programmer to join our team. As a senior member of our clinical study report development team, you will be responsible for creating high-quality clinical study reports using your programming expertise.

Key Responsibilities:

  1. Importing and Validating Data: Import data from various sources and perform quality control checks to ensure accuracy and completeness.
  2. Developing Programming Specifications: Interpret project-level requirements and develop detailed programming specifications.
  3. Coding and Testing: Write programming code in SAS, following established Good Programming Practices, and validate datasets and statistical outputs.
  4. Communicating and Collaborating: Work closely with internal and client statisticians and clinical team members to ensure understanding of requirements and timelines.

Requirements:

  • Bachelor's or Master's degree in Biostatistics, Statistics, Mathematics, or Computer Science.
  • 5+ years of experience in Statistical Programmer role from CRO/Pharma with ADaM and TFL.
  • Excellent accuracy, attention to detail, problem-solving, organizational, and interpersonal communication skills.

Benefits:

  • A competitive estimated salary of $90,000 - $120,000 per year, depending on experience and location.
  • Opportunities for professional growth and development.
  • A dynamic and collaborative work environment.


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