(高级）临床监查员 ID134115

You will be managing competing priorities, supporting the on-site team, ensuring investigators follow the clinical trial protocol, providing training, and most importantly, motivating the team to ensure high quality results.

The Role and your Responsibilities

- To assist the study management teams in completion of all required tasks

- To have thorough understanding of clinical trials

- To assist project teams with study specific documentation and guidelines as appropriate

- To contribute to the creation of CTMS guidelines and provide training on them

- To assist in co-ordination of investigator payments, if applicable

- To co-ordinate document translation, if required

- To assist with the coordination of team member tracking;

You are:

Education (minimum/desirable):A degree in a scientific or health care discipline preferred.

Languages: Fluent English (oral and written).

Experience/Professional requirement:

- Solid medical and business knowledge.

- at least 1 years CRA experience.

- Knowledge and experience in international (FDA, EMEA) and local regulations.

- Good communication skills

- Ability to manage multiple priorities

- Computer literacy.