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The successful candidate will be responsible for all aspects of a clinical study including but not limited to - Site selection and study start up, regulatory and ethics and submissions, feasibility's, patient and physician recruitment, monitoring, investigator meetings and study close out activities as well as overseeing a team Junior CRA's.
You must be ICH - GCP compliant and have a clinically focused working background and hands on monitoring experience within a previous role.
You will be working on Phases II to IV of a clinical trial and will be responsible for clinical studies in different therapy areas.
As part of this globally established clinical trial focused organisation you will be given the opportunity to grow and develop your clinical career with a specific career development programme designed specifically for CRA's.
In addition you will be rewarded with a competitive basic salary along with other industry standard benefits including - Private Health-care, Life insurance, Pension Scheme, Mobile Phone , Lap top, Childcare vouchers and discounted gym membership.
This is an excellent opportunity for someone to progress their clinical career long term within one of the industries top organisations