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. PSI is a leading Contract Research Organization with more than 25 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. Originally posted on Himalayas