Principal Clinical Data Standards Consultant

icon· 647 ICON Clinical Research (Beijing No. 2) Co., Ltd.
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📍 China, Beijing📍 China, ShanghaiFull time

About this role

China-Principal Clinical Data Standards Consultant

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


Principal Data Standards Consultant

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

Principal Data Standard Consultant

China

As a Principal Clinical Data Standards Consultant at ICON Plc, you will:

  • Provide expert-level functional knowledge in at least one standards domain, contributing to the development of standards content both internally and for sponsor-facing projects.
  • Develop, implement, and maintain ICON Data Collection standards libraries in compliance with CDISC, sponsor, and regulatory requirements.
  • Act as a subject matter expert to guide standards implementation and ensure compliance across clinical data management activities.
  • Apply deep understanding of business challenges to recommend and drive best practices, improving processes, products, and services to enhance competitive differentiation.
  • Collaborate cross-functionally to define data collection strategies and standards for clinical trials.
  • Participate in standards governance activities, influencing decision-making and providing expert input on complex topics.
  • Lead or contribute to departmental initiatives, potentially acting as a project lead with responsibility for coordinating team members.
  • Support the development of training materials and reference documentation across standards topics such as CDASH & Controlled Terminology.
  • Stay up to date with industry trends, regulatory changes, and emerging standards, ensuring continuous improvement of ICON practices.
  • Provide mentorship and guidance to more junior team members.
  • Supporting a Chinese language version of ICON Standards library and serve as SME for studies in China.

Requirements:

  • A Bachelor’s degree in a relevant discipline (e.g., Life Sciences, Computer Science, or similar); advanced degrees are advantageous.
  • Approximately 8+ years of experience in clinical data management, with significant expertise in data standards.
  • Advanced proficiency in CDISC standards (CDASH, SDTM, Controlled Terminology, etc.)  and strong knowledge of regulatory requirements (FDA, EMA, etc.).
  • Proven experience with EDC build/design tools, such as Medidata Rave and/or Veeva Vault EDC/CDMS.
  • Demonstrated ability to solve complex problems, using advanced analytical thinking and sound judgment to develop innovative solutions.
  • Strong leadership capabilities, including experience leading initiatives or mentoring team members.
  • Excellent interpersonal, communication, and influencing skills, with the ability to present, defend analyses, and secure stakeholder alignment on complex topics.
  • Ability to significantly impact operational, project, or departmental objectives, ensuring delivery of high-quality outcomes aligned with business strategy.

If you are ready to make a meaningful impact in the field of clinical data standards and contribute to innovative, high-impact clinical projects, we encourage you to apply and join ICON’s growing team.


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

Frequently Asked Questions

Is the salary disclosed for the Principal Clinical Data Standards Consultant position at icon?
The salary for this Principal Clinical Data Standards Consultant role at icon is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Principal Clinical Data Standards Consultant position at icon located?
This Principal Clinical Data Standards Consultant role at icon is based in China, Beijing, China, Shanghai. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Principal Clinical Data Standards Consultant role at icon full-time or part-time?
This is listed as a Full time position. It is posted as a Principal Clinical Data Standards Consultant role in the 647 ICON Clinical Research (Beijing No. 2) Co., Ltd. department at icon.
Which team or department does the Principal Clinical Data Standards Consultant at icon belong to?
This Principal Clinical Data Standards Consultant position is part of the 647 ICON Clinical Research (Beijing No. 2) Co., Ltd. department at icon. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Principal Clinical Data Standards Consultant position at icon?
Click the "Apply Now" button on this page. You will be redirected to icon's official application portal hosted on workday where you can submit your application directly.
When was the Principal Clinical Data Standards Consultant job at icon posted?
This Principal Clinical Data Standards Consultant position at icon was posted on Jul 24, 2026. Apply as soon as possible — early applications are often reviewed first.
Principal Clinical Data Standards Consultant
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