Clinical Site Associate Job at ICON Plc | Apply Now
A Clinical Site Associate Job at ICON has opened in Taipei for aspiring clinical research professionals. This hybrid role offers an opportunity to support site management activities and ensure the efficient conduct of clinical trials. Interested candidates are encouraged to apply soon.
- Position: Clinical Site Associate
- Location: Taipei, Taiwan
- Job Reference: JR152809
- Department: Clinical Monitoring
About ICON
ICON is a global healthcare intelligence and clinical research organization dedicated to bringing new medicines and treatments to patients faster. With a strong focus on integrity, collaboration, agility, and inclusion, ICON is committed to fostering a culture that values its employees and partners.
Clinical Site Associate Job Description
In this Clinical Site Associate Job at ICON, the individual will support site management activities, ensuring that clinical trials are conducted efficiently, compliantly, and to the highest quality standards. This role involves contributing to scientific operations activities and collaborating with various teams to achieve deliverables.
Eligibility Criteria
- Bachelor’s degree in life sciences or a related field, or equivalent experience.
- Initial experience in clinical research, administration, or a similar regulated environment is preferred.
- Strong organizational skills with the ability to manage multiple tasks, priorities, and deadlines.
- High attention to detail and accuracy in documentation and data entry.
- Effective written and verbal communication skills, with a customer-focused approach to site support.
- Proficiency with MS Office and comfort working with electronic systems and databases.
- Ability to work collaboratively in a team environment and adapt to changing priorities.
- Willingness to travel as required (approximately 10%).
Key Responsibilities
- Supporting site activation activities, including the collection, review, and tracking of essential documents and approvals.
- Maintaining up-to-date site information and status in clinical trial management systems and trackers.
- Assisting CRAs and project teams with site communications, follow-up, and resolution of site-level queries.
- Coordinating logistics for site visits and meetings, including scheduling, documentation preparation, and follow-up actions.
- Ensuring accurate filing and maintenance of essential documents to support inspection and audit readiness.
- Collaborating with internal stakeholders to support timely site payment processing and issue resolution.
- Contributing to process improvement initiatives and sharing best practices to enhance site support efficiency.
This Clinical Site Associate position at ICON in Taipei is an excellent chance for qualified candidates to contribute to impactful clinical research. Interested individuals are encouraged to apply before the deadline to seize this opportunity.
