Position overview:
As a Clinical Research Associate (CRA) 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;
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.