Description
Syneos Health is seeking a CRA II to join their team in Beijing.
The successful candidate will be responsible for conducting on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.
Key responsibilities include:
- Conducting on-site and remote monitoring of clinical research studies
- Developing and implementing tools, procedures, and processes to ensure quality monitoring
- Contributing to the design, implementation, and delivery of processes, programs, and policies
- Managing defined components of projects or processes within the area of responsibility
- Ensuring accurate and timely documentation of monitoring activities and findings
- Collaborating with cross-functional teams to support clinical trial operations
The ideal candidate will have:
- A Bachelor's degree in a related field or equivalent experience
- Minimum of 2-4 years of experience in clinical research monitoring
- Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements
- Excellent communication and interpersonal skills
- Ability to work independently and manage multiple priorities
- Proficiency in using clinical trial management systems and other relevant software
Preferred certifications include:
- Certified Clinical Research Associate (CCRA) or equivalent certification
Necessary skills include:
- Attention to detail and strong analytical skills
- Problem-solving abilities and critical thinking
- Ability to work effectively in a team environment
- Strong organizational and time management skills
- Proficiency in Microsoft Office Suite