Clinical Resource coordinator
- Contract Type
Role: Clinical Research Coordinator
Location: Riverside, California (USA)
My client, an established research site that have been about for over 10 years are looking to add a Clinical Research Coordinator to their team. They have sites across California and focus on medical studies and CNS studies within the industry. This Clinical Research Coordinator will have the ability to work very closely with the team and site manager whilst engaging in patient interaction.
The right candidate (Clinical Research Coordinator) will be able to come directly into the site and effectively coordinate the project at a moment’s notice. This client prides themselves in coordinating trials both as ethically and as professionally as possible. Your time in this company will be exciting and fast changing so your strategic input will not be under-valued!
(this is an example of some of the responsibilities but your role will not be limited to solely the below)
Closely collaborate with the manager of the project
Assist more junior Coordinators
Assist the clinical study team with blind trials, shipping the study documents and news letters
Tracking study tools
Travel may be needed
YOU WILL NEED:
2+ years’ experience as a Clinical Research Coordinator
Understanding of FDA regulations and good clinical practice (GCP)
Must be Registered Nurse
Develop your career
Be part of an ethical business
A competitive package
This is a superb opportunity to get in to a business that is going straight to the top and be a valued member right from the start. If you want clear career progression and want to find more about this exceptional opportunity, then send me your CV with a cover letter to email@example.com.
If you or anyone you know may be looking for a different opportunity and want specialist help than feel free to get in touch with anyone with in my team for a friendly consultation to explore the market!