Clinical Research Associate/Senior Clinical Research Associate

компания "oct, russia" we are looking for a clinical research associate to join our team. this position presumes primarily responsibilities of monitoring (pre-study, initiation, routine, and close-out visits) of investigator sites for the compliance to the study protocol, ich gcp, company’s sops and applicable regulations. job responsibilities: conduct and reporting of pre-study, initiation, routine monitoring and closeout visitscommunication with investigational sites and sites management ensuring the integrity of clinical data in adherence to all applicable regulatory guidelines, company’s sops and project-specific operating procedures assistance in feasibility studies negotiations of clinical trials agreements with the investigator sites and study budgets obtaining and review of required study documents from investigational sites project-specific training of sites and teams requirements: md or university degree in life sciences minimum a year of independent monitoring experience in clinical trials fluent english, written and spoken ability to travel at least 60-65% of working time experience in oncology projects is a plus we offer: fixed term employment contract (maternity cover) challenging job in a highly qualified team employee-friendly work environment competitive salary professional growth in clinical research