Clinical Research Associate II

As a Clinical Research Associate II 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 (if applicable) - 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 - Participate in feasibility research - 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 in North America. - Experience in all types of monitoring visits in Phase II and/or III - Full working proficiency in English and French. - Proficiency in MS Office applications - Ability to plan, multitask and work in a dynamic team environment - Communication, collaboration, and problem-solving skills - Ability to travel - Valid driver’s license 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 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. Originally posted on Himalayas