We are currently looking to strengthen our Clinical Monitoring team in Spain and are seeking CRA III for our Oncology department to be based in our Madrid or Barcelona office.
We can also accept home office based workers too. Core responsibilities:
A brief summary of duties you will be involved in:
· Monitoring all types of clinical trials and participating in all types of site visits ensuring adherence to Good Clinical Practices, investigator integrity and compliance with all study procedures · Data Handling, Reporting, Tracking and administrative tasks · Performing management of study site activities to ensure the integrity of clinical data, in adherence to all applica ...