Senior CRA

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 SIV, RMV, COV onsite monitoring visits 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 Prepare and particiapte on audits and inspections College/University degree in Life Sciences or an equivalent combination of education, training & experience Independent on-site monitoring experience Experience in all types of monitoring visits in Phase II and/or III Experience in Oncology is a plus Full working proficiency in English and French is essential. 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.