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Clinical Research Associate

  1. Taipei
JR135128
  1. Clinical Monitoring
  2. ICON Strategic Solutions
  3. Office Based

About the role

Clinical Research Associate (Phase IV trials)

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

Job Description

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

Qualification

  • Bachelor's degree in life science courses (Pharma, Biology, Medical Science, Nursing, etc)
  • At least 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 Chinese 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 maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. 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 or submit a request here

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.

Are you a current ICON Employee? Please click here to apply

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