Clinical Research Associate II

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. You will: • Conduct and report all types of onsite monitoring visits • Be involved in study startup and feasibility research • Perform CRF review, source document verification and query resolution • Be responsible for site communication and management • Be a point of contact for in-house support services and vendors • Communicate with internal project teams regarding study progress • Support regulatory team in preparing documents for study submissions • College/University degree in Life Sciences or an equivalent combination of education, training & experience • Independent on-site monitoring experience Argentina • Experience in all types of monitoring visits in Phase II / III • Experience in Oncology is preferred • Full working proficiency in English and Spanish • Proficiency in MS Office applications • Ability to plan and work in a dynamic team environment • Communication, collaboration, and problem-solving skills • Ability to travel This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.