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Clinical Site Associate

  1. Taipei
JR136044
  1. Clinical Monitoring
  2. ICON Full Service & Corporate Support
  3. Office or Home

About the role

Clinical Site Associate - Taiwan- Office Hybrid

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.

We are currently seeking a Clinical Site Associate to join our diverse and dynamic team. As an IHCRA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.

• Recognize, exemplify and adhere to ICON’s values which centre on our commitment to People, Clients and Performance.
• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our process to add value to our business and meeting client needs.
• *Become familiar with ICON’s SOPs/WPs, ICH GCP guidelines and appropriate regulations.
• *Become familiar with ICON systems
• *Maintain timelines and ensure accuracy and completeness of data entered into ICON systems 
• Become familiar with the principles of and assist with investigator recruitment
• *Serve as the primary in-house contact for sites and investigators participating in studies
• *Conducts and completes remote site management activities, with support as needed, according to applicable SOPS and the Study Monitoring Plan.
  *To contact Clinical sites for specific requests  (e.g. enrolment updates, missing documentation, data entry timeliness, data query follow-up,  CDA finding follow-up,  and action Item resolution or other sponsor specific CRA tasks.
• *Takes responsibility for project tasks and sees these tasks through to successful completion, with support. 
• *Maintains a professional interpersonal relationship with study team, sites, and Sponsor.
• *Participates in QA Audits as needed.
• *Regularly attends and contributes to project specific and departmental meetings
• *Ability and willingness to travel as needed (drive and fly)
•Maintains Sponsor and patient confidentiality
•To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.  The requirements listed below are representative of the •knowledge, skill and/or ability required.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions if feasible for the role.
•Ability to liaise successfully and interact positively with clinical project teams, customers, site staff and all levels of staff across relevant departments.
•Effective prioritization skills, ability to multi-task and meticulous attention to detail.
•Comprehensive knowledge and understanding of ICH-GCP and other relevant regulations for the conduct of clinical trials related to pharmaceuticals, biologics, medical devices and combination products.
•Competent computer skills
•Good oral and written communication skills
•Due to the nature of this position, it may be required for the employee to travel.  Therefore dependent on the employee’s location, a valid driver’s license will be required
•Foreign language skills desirable
• Other duties as assigned

Your profile

  • Bachelor's degree in a relevant field, such as life sciences or healthcare
  • Previous experience in clinical research or a related field preferred
  • Strong organizational and communication skills
  • Ability to work independently and collaboratively in a fast-paced environment
  • Attention to detail and ability to prioritize tasks effectively

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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