FSP-(Senior) Unblinded Clinical Research Associate- Remote in Taiwan
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.
As an
Unblinded CRA II at ICON, you will perform independent unblinded monitoring behind an established blinding firewall, oversight of Investigational Product (IP) and pharmacy processes across sites—including international travel to Singapore—and contribute to the advancement of innovative treatments and therapies while maintaining strict trial integrity.
What You Will Do
You will contribute to unblinded clinical trial monitoring activities, taking responsibility for pharmacy oversight, IP accountability, and maintaining blinding integrity while working collaboratively with sponsor and site pharmacy teams.
Key Responsibilities Include
- Conducting unblinded site qualification, initiation, routine monitoring, and close-out visits in local and international sites (specifically Singapore), focusing on pharmacy processes and IP management.
- Ensuring protocol compliance, IP accountability, temperature log verifications, and patient safety throughout the trial process without compromising trial blinding.
- Collaborating with site pharmacists and pharmacy staff to facilitate smooth study conduct, unblinded dispensing, and proper IP disposal/return.
- Performing unblinded data review, pharmacy documentation checks, and resolution of pharmacy queries to maintain high-quality clinical data in restricted access spaces (e.g., uMVRs).
- Contributing to the preparation and review of unblinded study documentation, including pharmacy manuals, unblinded monitoring plans, and IP destruction logs.
Your Profile
You will bring relevant clinical trial monitoring experience with a focus on unblinded/pharmacy oversight, along with the following qualifications and skills.
Required Qualifications And Experience
- Bachelor's degree in Pharmacy, Life Sciences, or a healthcare-related field (Registered Pharmacist license preferred).
- Minimum of 2 years of experience as a Clinical Research Associate, including independent site monitoring visits.
- In-depth knowledge of clinical trial processes, unblinded monitoring procedures, local regulations (including HSA Singapore guidelines), and ICH-GCP guidelines.
- Strong organizational, integrity-driven, and communication skills, with meticulous attention to detail regarding IP management.
- Ability to work independently and maintain strict blinding firewalls in a fast-paced environment.
- Willingness and flexibility to travel as required, including regular regional travel to Singapore (approximately 50% in Taiwan or to Singapore).
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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.
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