Description
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a Clinical Research Associate, China at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
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.
Your Profile
- Bachelor's degree in a scientific or healthcare-related field.
- Prior experience or strong interest in clinical research.
- Knowledge of clinical trial processes, regulations, and guidelines.
- Excellent organisational and communication skills.
- Ability to work collaboratively in a fast-paced environment with attention to detail.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance-related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways