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Principal Clinical Data Standards Consultant

ICON PLC

Principal Clinical Data Standards Consultant

Salary Not Specified

ICON PLC, City of Westminster

  • Full time
  • Permanent
  • Onsite working

Posted 2 weeks ago, 4 Sep | Get your application in now before you miss out!

Closing date: Closing date not specified

job Ref: 4b0367cfb8a041f08ef498ec04743bb2

Full Job Description

  • As a Senior Clinical Data Standards Consultant at ICON Plc, you will be responsible for:

  • 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., Various annual leave entitlements

  • A range of health insurance offerings to suit you and your family's needs.

  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.

  • Life assurance

  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.


    • Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.

  • A Bachelor's degree in a relevant field (e.g., Life Sciences, Computer Science, or related discipline); advanced degrees are a plus.

  • Extensive experience in clinical data management and standards within the pharmaceutical or biotechnology industry.

  • Advanced Proficiency in CDISC (Clinical Data Interchange Standards Consortium) standards and relevant regulations (e.g., FDA, EMA).

  • Excellent analytical and problem-solving skills with a keen attention to detail.

  • Excellent communication and collaboration abilities to work effectively in cross-functional teams.

    ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

    In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.