Job overview
in this role, you will collaborate with a dynamic team to identify and select investigational sites for clinical studies. Your primary responsibility will be to ensure adherence to applicable regulations and principles of ich-gcp.
* independent monitoring of studies with a proactive approach to quality management
* submission of protocol and consent documents for ethics approval
* balancing sponsor-generated queries and ensuring study efficiency
to succeed in this position, you should possess the following skills:
* at least 24 months of experience in oncology trials as a clinical research associate
* advanced english proficiency for effective communication
* a college degree in medicine, science, or equivalent field
* familiarity with ich-gcp guidelines and ability to review medical data
* excellent written and verbal communication skills for collaboration
about this opportunity
this is a fantastic chance to develop your career in clinical research operations. If you have a passion for detail, enjoy working in a fast-paced environment, and are committed to delivering high-quality results, we encourage you to apply.