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Clinical Research Associate (Real World Solution)

  1. Hong Kong
2024-115545
  1. Clinical Monitoring
  2. ICON Strategic Solutions
  3. Remote

About the role

This vacancy has now expired. Please see similar roles below...

As a Real World Evidence CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Working location: Hong Kong Homebased 


What you will be doing:

  • Design and/or implement a series of local/regional/global planned LDGs, HECON and Post Approval Studies/researches with customers:
    • Work closely with internal and external stakeholders to implement and track the studies timely with quality, within budget and compliant.
    • Plan and evaluate study timeline, fair market value, budget and all resource required
    • Communicate with study related team regarding budget allocation and executive plan.
    • Generate site feasibility questionnaire and conduct site feasibility visit to enroll qualified sites
    • Generate start-up plan to ensure study can be initiated according to planned timeline
    • Prepare IRB and RA submission dossier
    • Arrange study material allocation and delivery
  • Design and/or implement a series of local/regional/global planned Investigator studies and in scope research types with customers:
    • Conduct denied paries screening and anti-bribery/corruption checks
    • Ensure Fair Market Value assessment is completed as appropriate
    • Negotiate contracts and budget with investigators and hospitals
    • Send quarterly status update report request
    • Ensure study database is updated and maintained throughout the study phase
    • Provide professional guidance to investigators
  • Maintain good relationship with site personnel
  • Involve and/or conduct audit, inspections and other quality assurance activities
  • Contribute to Medical Scientific Affairs operational excellence

You are:

  • Bachelor's degree in life science courses (Pharma, Biology, Medical Science, Nursing, etc)
  • Prefer 1-3 years of handling experience in clinical trials or investigator-initiated studies
  • Strong project management skills and sense of urgency
  • Clinical study execution related knowledge, including but not limited to GCP, GPP, IRB submission, etc.
  • Demonstrate ethics and integrity
  • Driven result, focus on customers and patients
  • Proficiency in Cantonese and English


What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others



Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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