Clinical Site Associate Job at ICON Plc | Apply Now
A rare chance for aspiring professionals to apply for a Clinical Site Associate Job at ICON in Seoul. This role offers an opportunity to contribute to clinical trials, ensuring they are conducted efficiently and to the highest quality standards. Interested candidates are encouraged to apply soon.
- Position: Clinical Site Associate
- Location: Seoul
- Reference Number: JR152421
- Department: Clinical Monitoring
About ICON
ICON is a global healthcare intelligence and clinical research organization united by a mission to bring new medicines and treatments to patients faster. As a values-driven organization, integrity, collaboration, agility, and inclusion are at the heart of how ICON works and interacts with each other, customers, patients, and suppliers.
Clinical Site Associate Job Description
In this Clinical Site Associate Job at ICON, the individual will support site management activities and ensure that clinical trials are conducted efficiently, compliantly, and to the highest quality standards. The role involves contributing to scientific operations activities, taking responsibility for deliverables, and working collaboratively with various stakeholders.
Eligibility Criteria
The ideal candidate will bring relevant scientific operations experience, along with the following qualifications and skills:
- 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 Job presents a compelling opportunity for qualified candidates to contribute to meaningful clinical research. Interested individuals are encouraged to apply before the deadline to seize this opportunity.
