Clinical Research Associate

§ Ideally, a University or college degree (life science preferred)
§ Have typically 1-2 years experience as a clinical monitor; experience in non-interventional studies might be an advantage
§ Experience in working with eCRF or solid PC skills
§ A thorough knowledge of Good Clinical Practice (GCP) and Good Epidemiology Practice Guidelines
§ Willingness to travel "

§ Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits and other duties.
§ Performs and coordinates all aspects of the clinical monitoring process in accordance with GCPs and global SOPs and study protocols.
§ Ensure the integrity of the data submitted

Compania ofera consultanta in domeniul marketingului farmaceutic si in resurse umane.
Postul este oferit de o companie franceza producatoare de medicamente originale.