Clinical Data Standards Consultant Lead

4 days ago

Reading, Reading, United Kingdom Icon plc Full time

About ICON plc

ICON plc is a world-leading healthcare intelligence and clinical research organization.

We are proud to foster an inclusive environment driving innovation and excellence, and we welcome talented individuals to join us on our mission to shape the future of clinical development.

Job Summary

We are currently seeking a Principal Clinical Data Standards Consultant to join our diverse and dynamic team.

As a Clinical Data Standards Consultant at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Key Responsibilities

  • Developing tools to aid in the implementation and compliance of CDISC, Sponsor, and ICON standards.
  • Collaborating with cross-functional teams to define data collection strategies and standards for clinical trials.
  • Developing and maintaining training and reference materials related to standards topics including CDASH, SDTM, Terminology, ADaM, define-XML and regulatory submission requirements.
  • Managing the development and maintenance of data management processes and tools.
  • Keeping abreast of industry trends and regulatory updates related to data standards and ensuring their integration into ICON's practices.

Requirements

  • A Bachelor's degree in a relevant field (e.g., Life Sciences, Computer Science, or related discipline).
  • Extensive experience in clinical data management and standards within the pharmaceutical or biotechnology industry.

About Working at ICON

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

We offer a range of benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities for you and your family.

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