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ICON

Clinical Trial Liaison

China, Beijing · China, Shanghai

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hirly's read of this role

Seniority
Mid level
Country
CN
Work mode
On-site / unstated
First seen by hirly
27 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

  • Clinical Trial Liaison, China, Home based
  • 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 Trial Liaison to join our diverse and dynamic team. ICON’s field-based Clinical Trial Liaisons are highly trained site engagement specialists who support clinical trials by providing scientific and clinical support to investigators and site staff to ensure study sites have a thorough understanding of the study design and procedures so that clinical trial goals are achieved. The CTL also functions as a recruitment specialist in developing and optimizing strategies at site and study level to drive successful patient enrolment.

Must have

Ability to travel up to 75%-80%. (Mostly Domestic)

Doctoral degree (M.D., PharmD, or PhD) is required.

Fluent in Chinese and English

What you will do:

Collaborate with cross-functional teams to design and implement effective clinical trial enrollment strategies.

Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards.

Foster strong relationships with study sites and investigators to enhance patient recruitment and retention.

Act as a liaison between sponsors, investigators, and study participants, providing support and guidance throughout the enrollment process.

Contribute to the continuous improvement of enrollment processes and strategies to optimize trial outcomes.

Cultivate relationships and recruit the most appropriate sites to participate in trials

Your profile:

Experience in a clinical research environment in Pharma, Biotech, or CRO in scientific and/or clinical operations is preferred

Proven experience in clinical trial enrollment or related roles.

Experienced in local healthcare landscape

Ability to discuss and apply technical/scientific/clinical knowledge

Strong analytical and problem-solving skills with the ability to interpret complex medical data.

Broad scientific and medical knowledge with an understanding of clinical development

Excellent interpersonal skills with the ability to develop relations with internal and external stakeholders

Proactive and self-motivated with the demonstrated ability to work collaboratively and independently

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

Original posting on ICON's site ↗

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