Clinical Site Associate Job at ICON Plc | Apply Now
The Clinical Site Associate Job at ICON plc in Shanghai offers aspiring candidates an opportunity to contribute to clinical trials while ensuring compliance and quality standards are met. Interested candidates are encouraged to apply before the deadline.
- Position: Clinical Site Associate
- Location: Shanghai, China
- Reference Number: JR155976
- Department: Clinical Monitoring
About ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization. The company is dedicated to fostering an inclusive environment that drives innovation and excellence in clinical development. With a commitment to shaping the future of clinical research, ICON operates globally, providing a range of services to support clinical trials.
Clinical Site Associate Job Description
In this Clinical Site Associate Job at ICON, the successful candidate will support site management activities, ensuring that clinical trials are conducted efficiently and to the highest quality standards. This role involves contributing to scientific operations activities and collaborating with various stakeholders to enhance site support efficiency.
Eligibility Criteria for Clinical Site Associate Job
- 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 organisational 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.
What ICON can offer you
ICON prioritizes building a diverse culture that rewards high performance and nurtures talent. In addition to a competitive salary, ICON offers a range of benefits designed to support well-being and work-life balance for employees and their families. Benefits include various annual leave entitlements, health insurance offerings, retirement planning options, and access to a global network of professionals through the Global Employee Assistance Programme.
This Clinical Site Associate Job at ICON plc in Shanghai is a significant step for those looking to advance their careers in clinical research. Qualified candidates are encouraged to apply at the earliest to seize this chance.
