Clinical Job Opportunity at ICON: Apply Now for a Clinical Trial Associate role in Beijing
If you are searching for a promising clinical job in global research, this opportunity at ICON could be the right fit. This role as a Clinical Trial Associate in Beijing allows professionals to work with a leading clinical research organization while contributing to innovative treatments. As part of ICON careers, this position is ideal for candidates exploring jobs in China within the clinical research and healthcare intelligence space.
Job Details:
- Job Position: Clinical Trial Associate
- Company Name: ICON plc
- Location: Beijing, China
- Job ID: JR141425
Qualifications:
- Bachelor’s degree in a healthcare-related field.
- Prior experience or strong interest in clinical research or a Clinical Trial Associate role.
- Knowledge of clinical trial processes, regulations, and guidelines.
- Excellent organizational and communication skills.
- Ability to work collaboratively in a fast-paced environment with strong attention to detail.
About the Company:
ICON plc is a world-leading healthcare intelligence and clinical research organization. ICON careers are built on fostering an inclusive environment that drives innovation and excellence. By joining ICON, professionals can contribute to shaping the future of clinical development through meaningful clinical job opportunities worldwide.
Job Description:
This clinical job supports the ICON Full Service & Corporate Support teams. ICON is currently seeking a Clinical Trial Administrator to join its diverse and dynamic workforce. In this Clinical Trial Associate role, you will assist with the design and analysis of clinical trials, interpret complex medical data, and contribute to the advancement of innovative treatments and therapies.
Key Responsibilities:
- Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
- Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
- Support the preparation of study-related materials, such as informed consent forms and case report forms.
- Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
- Contribute to the tracking and reporting of clinical trial metrics and milestones as part of this clinical job.
