This is an exciting opportunity with an established and growing organisation specialising in supplying services and products to clients world wide. They are looking for an experienced Clinical Research Associate to join their team. Reporting to the Clinical Operations Manager, responsibilities will include:
To ensure appropriate attention is provided to the sites in order to drive data quality so that the clinical study protocol requirements are fulfilled within the appropriate regulatory and ethical framework.
Experience of performing site start up procedures, routine monitoring and site closure.
Ability to manage multiple priorities across various clinical trials
Establishing regular lines of communication plus administering protocol and related study training to assigned site
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
A Bachelor's degree in a health care or other scientific discipline or educational equivalent or nursing degree
Alternatively, you should have an equivalent combination of education, training and experience
Must have at least 2 years of monitoring experience as CRA
Case Report Forms
Certified Radiology Administrator
Clinical Research Associate
Certified Retirement Administrator