Senior Clinical Research Associate

Your responsibilities will include: Conducting and reporting all types of onsite monitoring visits 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 BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience Independent on-site monitoring experience in Slovakia Demonstrable experience in all types of monitoring visits in Phase II and III Fluency in Slovak and English Experience supporting Oncology and Gastroenterology studies is beneficial Valid driver's license and the ability to travel Intermediate to Advanced knowledge of MS Office Communication, collaboration, and problem-solving skills are essential PSI is a leading Contract Research Organisation with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way. We will guide and support you with information, making your experience as smooth as possible.