Overview

As a Clinical Trial Manager you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures.

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;

What is Required

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

Languages: Fluent English (oral and written).

Experience/Professional requirement:

1. Solid medical and business knowledge.

2. at least 5 years CRA experience and 1 year project management experience

3. Knowledge and experience in international (FDA, EMEA) and local regulations as well as Novartis standards.

4. Good communication skills

5. Ability to manage multiple priorities

6. Computer literacy.

职位福利：五险一金、年底双薪、交通补助、带薪年假、补充医疗保险、节日福利、弹性工作、定期体检