Principal Clinical Data Standards Consultant

Reposted 25 Days Ago
Be an Early Applicant
2 Locations
In-Office
Expert/Leader
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
Lead clinical data standards consulting: implement and maintain CDISC-based standards (CDASH/SDTM/ADaM/define-XML), develop tools, processes and training, collaborate cross-functionally, manage delivery and team capability, and ensure regulatory compliance for clinical trials.
Summary Generated by Built In
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

Skills Required

  • Bachelor's degree in life sciences, computer science, or related discipline
  • Extensive experience in clinical data management and standards within pharmaceutical or biotechnology industry
  • Advanced proficiency in CDISC standards and related specifications (CDASH, SDTM, ADaM, define-XML)
  • Knowledge of regulatory requirements related to data standards (e.g., FDA, EMA)
  • Consulting and advisory services experience, with ability to manage priorities and develop a team
  • Experience developing tools and maintaining data management processes and tools
  • Experience developing and maintaining training and reference materials on standards topics
  • Excellent analytical and problem-solving skills with attention to detail
  • Excellent communication and collaboration abilities for cross-functional teamwork
  • Willingness to travel as required (approximately 15%)
  • Legal right to work in the country where the role is based

ICON plc Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ICON plc and has not been reviewed or approved by ICON plc.

  • Healthcare Strength Benefits are described as comprehensive, with medical coverage and wellness initiatives highlighted. Larger sites are also associated with added wellness supports such as onsite fitness options and access to an employee assistance program.
  • Leave & Time Off Breadth Time-off and flexibility provisions are positioned as a meaningful part of the total package, including vacation/annual leave and flexible work scheduling. Flexibility is sometimes cited as helping offset long hours in certain roles.
  • Retirement Support Retirement and savings support is presented as a core component of the benefits package, including offerings such as pension arrangements in some locations and a U.S. 401(k) plan with company match. Financial planning resources are also emphasized as part of broader security benefits.

ICON plc Insights

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The Company
HQ: Dublin
34,685 Employees
Year Founded: 1990

What We Do

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

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