Job Details

Parexel Clinical Monitoring/Site Management Opportunity

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Key Accountabilities:

• Monitoring and Management of Investigator Sites
• Data Quality
• Reporting
• Documentation
• Compliance with Parexel standards

Skills:

• Computer Literacy (word processing and spreadsheets, PowerPoint)
• Proficient in Chinese, good command of written and spoken English is required
• Good interpersonal skills, good at communication
• A flexible attitude with respect to work assignments and new learning, quickly-learning
• Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
• Willingness to work in a matrix environment and to value the importance of teamwork

Knowledge and Experience:

• At least 1.5 years (2 years preferable) of Clinical Monitoring/ Site Management experience, global study monitoring experience is preferred
• Good knowledge of ICH/GCP, relevant international and local regulations relating to Clinical Research
• Degree in Life Science, Nursing, Pharmacy, or other relevant education background
• Bachelor's degree or above, or equivalent