Monitor and own the progress of clinical studies at investigative sites, ensuring clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Coordinate activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
Job listings
$44,613–$74,466
USD/year
Performs and coordinates all aspects of the clinical site monitoring services, assessing for protocol and regulatory compliance. Responsibilities include driving investigative site and patient recruitment, conducting source data verification, assessing drug accountability, data collection, (regulatory) document collection, performing qualification, initiation, monitoring and close out visits at investigational sites.
The Clinical Trial Liaison (CTL) role is designed to transform the clinical research site experience by making the customer experience a priority. This strategic role serves as a critical interface between the organization and clinical research sites, focusing on therapeutic area networking, site outreach, education, specialized training, and enrollment acceleration.
Parexel is seeking Clinical Research Associates with at least 12 months recent oncology experience to be dedicated to a single sponsor. Manageable sites and protocols are the mantra, offering exciting challenges with time for your outside life. The role involves site management and monitoring activities across assigned oncology studies, working with industry leaders and world-class technology.