Job Description
Job Description
As a Senior Clinical Research Associate you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.
You will:
Conduct and report all types of onsite monitoring visits Be involved in study startup (if applicable) Perform CRF review, source document verification and query resolution Be responsible for site communication and management Supervise study activities, timelines, and schedules on the country level Be a point of contact for in-house support services and vendors Be involved in quality control, such as compliance monitoring and reports review Participate in feasibility ...