Job Responsibilities

- To initiate, monitor and close up clinical studies in compliance with study protocols and company's guidance;
- To document and archive all clinical trial relevant activities, verify the accuracy, completeness and legibility of the data collected in the studies
- Periodically report/update any study specific tracking systems of sites and update IMPACT database for responsible sites.
- To propose the potential investigational sites to clinical affairs manager for a specific study, verify the quality of the investigator and the suitability of the sites;
- To support study managers to manage and negotiate with external service providers
- To ensure a smooth communication through the studies between the company and sites, report any studies related issues to the line manager in a timely manner.
- To join or aid in the training for junior monitoring staff.

Requirements:

- Bachelor or above Degree in medicine, pharmacy science;
- More than 3 years clinical monitoring experience in line with ICH GCP;
- Self-motivated, excellent interpersonal skills, negotiation skills and presentation skills;
- Good communication skills with fluent verbal and written English and Chinese;
- Willing to work at sites and can travel frequently;
- Teamwork spirit;