Senior Clinical Research Associate

As a Senior CRA 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.Office-Based or Home-basedYou will:Conduct and report all types of onsite monitoring visitsBe involved in study startup (if applicable)Perform CRF review, source document verification and query resolutionBe responsible for site communication and managementSupervise study activities, timelines, and schedules on the country levelBe a point of contact for in-house support services and vendorsBe involved in quality control, such as compliance monitoring and reports reviewParticipate in feasibility researchSupport regulatory team in preparing documents for study submissions