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. Your focus will be on subjects’ rights, safety and well-being and quality of data compliance. This is a freelance (contractor) home-based position Your responsibilities will include: Conducting and reporting all types of onsite monitoring visits Driving the study startup phase (if applicable) Performing CRF reviews, source document verification and query resolution Be responsible for site communication and management Supervising study activities, timelines, and schedules for each site Acting as a point of contact for in-house support services and vendors Supporting quality control, such as compliance monitoring and reports review Participating in feasibility research Supporting the regulatory team in preparing documents for study submissions and regulatory approval BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience Independent on-site monitoring experience in Slovakia, ideally on multiple projects at a time Demonstrable experience in all types of monitoring visits in Phase II and/or III Strong written and verbal communication skills Fluency in Slovak and English Experience supporting Oncology studies is beneficial, but not essential Int