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Clinical Trial Liaison

647 ICON Clinical Research (Beijing No. 2) Co., Ltd. · Beijing, China

Clinical TrialsImported listingfull-time1 day ago

About The Role

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

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

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

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Fluent in Chinese and English

What you will do

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  • Collaborate with cross-functional teams to design and implement effective clinical trial enrollment strategies.
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  • Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards.
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  • Foster strong relationships with study sites and investigators to enhance patient recruitment and retention.
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  • Act as a liaison between sponsors, investigators, and study participants, providing support and guidance throughout the enrollment process.
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  • Contribute to the continuous improvement of enrollment processes and strategies to optimize trial outcomes.
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  • Cultivate relationships and recruit the most appropriate sites to participate in trials

Your profile

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  • Experience in a clinical research environment in Pharma, Biotech, or CRO in scientific and/or clinical operations is preferred
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  • Proven experience in clinical trial enrollment or related roles.
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  • Experienced in local healthcare landscape
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  • Ability to discuss and apply technical/scientific/clinical knowledge
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  • Strong analytical and problem-solving skills with the ability to interpret complex medical data.
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  • Broad scientific and medical knowledge with an understanding of clinical development
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  • Excellent interpersonal skills with the ability to develop relations with internal and external stakeholders
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  • 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

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