Description
This individual will be responsible for managing clinical activities at Orthopedic Medical Device study sites conducting studies, as well as fostering strong, productive relationships with colleagues within the Organisation. Responsible for managing clinical study activities for multiple sites in single or several Clinical Projects. Oversees performance of appointed study sites conducting company initiated clinical studies.Responsible for the site visits, monitoring, communication and deliverables for the assigned study sites Serves as a member of the clinical study team and is the liaison between Clinical Operations and Study Site personnel for the specific clinical projects. Perform and coordinate all aspects of the clinical monitoring and site management. Medical Devices.
ROLE RESPONSIBILITIES
Performs and coordinates all aspects of the clinical monitoring and site management
Conducts site visits - assessing protocol and regulatory compliance, managing required documentation
Develops and maintaining collaborative relationships with investigational sites and client company personnel.
Leading on assigned clinical studies
Mentor, train and contribute to the development of junior clinical
SKILLS DESIRED
3 years experience working with medical devices
Good knowledge of FDA guidelines and GCP
Excellent communication skills
Strong attention to detail
LOCATION
South East England - With flexibility of home working.
This is an urgent requirement, and the ideal candidate will be able to start immediately. This is an excellent opportunity to work for a fast moving organisation, offering competitive daily/hourly rates. If you are interested in this position and would like some more information please call Hailey McDermott on and send an updated CV.
Please also pass this opportunity onto anybody you know who may be interested in this as we do offer £200 referral vouchers.
I look forward to hearing from you.