Clinical Data Coordinator

ICR United States USA

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Taiwan, Taipei China, Dalian (PRA) Until 8/22/2026 2+ years exp First posted November 3, 2025 Last posted December 23, 2025
Job description
CDC II

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.


We are currently seeking a Clinical Data Coordinator II to join our diverse and dynamic team. As a Clinical Data Coordinator II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies.

What you will be doing 

  • Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.
  • Manage clinical and third-party data reconciliation based on edit specifications and data review plans.
  • Tracks and communicates status of study and task metrics to clinical data scientist, project team, and functional management.
  • Address data related questions and recommend potential solutions.
  • Identify root cause to systematically resolve data issues.

Your profile 

  • Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.
  • Intermediate kNwledge of clinical data management within the pharmaceutical or biotechNlogy industry.
  • Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar).
  • Strong attention to detail and the ability to work effectively in a fast-paced environment.
  • Excellent communication skills and the ability to collaborate with cross-functional teams.
  • KNwledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.

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

About this role

Summary

Assist in managing and analyzing clinical trial data, ensuring data quality and compliance.

Job title

Clinical Data Coordinator II

Experience level

intermediate

Minimum experience

2+ years exp

Industry

healthcare

Location requirements

Taiwan, Taipei or China, Dalian; remote work not specified

Salary

Not specified

Management role

No

Skills & keywords

Required skills

clinical data managementdata validationregulatory guidelines

Preferred skills

MedidataOracle RDCICH-GCP

Specializations

clinical data managementdata validationmedical data
Locations

Structured locations inferred from the posting.

Taipei, Taiwan

Work arrangement unknown City

Dalian, Liaoning, China

Work arrangement unknown City
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