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From the employer's careers site First seen 10 Nov 2026

Feasibility Specialist, China

The employer hasn't listed a salary.

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Description

As a Senior Feasibility Specialist at ICON, you will evaluate and optimize the feasibility of clinical trials, ensuring they are well-planned and positioned for success.

You will lead on clinical research tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include:

  • Conducting in-depth feasibility assessments for clinical trials, including evaluating site capabilities, resource availability, and potential risks.
  • Collaborating with clinical operations teams, project managers, and other stakeholders to gather and analyze data relevant to trial feasibility.
  • Preparing comprehensive feasibility reports and recommendations to support project planning and decision-making processes.
  • Analyzing historical data and site performance metrics to identify trends, opportunities, and challenges impacting trial feasibility.
  • Developing and maintaining strong relationships with key stakeholders, including clinical sites, investigators, and external partners.
  • Staying up-to-date with industry trends, regulatory requirements, and best practices related to clinical trial feasibility and planning.
  • Providing mentorship and guidance to junior feasibility team members and contributing to continuous improvement efforts within the team.

You will have a strong foundation in clinical research, with the experience to work independently and guide others. Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience in clinical trial feasibility assessments, with a deep understanding of clinical research processes and site management.
  • Exceptional analytical skills, with the ability to interpret complex data and provide actionable insights.
  • Strong organizational and project management skills, with experience in handling multiple feasibility projects simultaneously.
  • Excellent communication and interpersonal skills, with the ability to build and maintain effective relationships with stakeholders at all levels.
  • Proficiency in data analysis tools and software relevant to feasibility assessments and clinical research.
  • Willingness to travel as required (approximately 15%)

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

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Skills

Required

  • clinical trial feasibility assessments
  • clinical research processes
  • site management
  • analytical skills
  • project management
  • communication and interpersonal skills
  • data analysis tools

Ready to apply?

You apply with the employer directly. Their original posting is here: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/China-Shanghai/Clinical-Trial-Associate_JR163766

Apply on ICON Strategic Solutions