Job Description

As a Clinical Research Associate you have a pivotal role in site management activities related to start up activities, regulatory compliance, patient enrolment, protocol adherence, CRF compliance and data quality for clinical programs for Roche products. You are responsible for: • Working according to ICH GCP, Roche policies and procedures, international ethical and scientific standards and local regulations • Performing on & off --site monitoring activities during study conduct to ensure adherence to Protocol, ICH-GCP guidelines, local regulatory requirements and SOPs • Proper handling of safety information • Proper collection and archiving of essential study documentation • Timely and accurately execution of monitoring plan and other reporting We strive to continuously improve our performance and you will be a pro-active player in optimizing processes and improving the quality level. The position will allow you to develop a broad spectrum of skills whilst at the same time obtain broad knowledge of the pharmaceutical industry. Personal development is an important and integrated part of career in our organization. The position is based in Tehran and is on local term and conditions.