Advance your career as a Clinical Research Associate for PSI, overseeing clinical trials and ensuring compliance with regulatory standards. Focus on patient enrollment and data integrity.PSI is looking for a qualified Clinical Research Associate with a strong background in site monitoring and clinical trial management. This role provides chance to work on diverse therapeutic indications while leading site training and monitoring efforts. Your expertise will help guide project timelines and ensure adherence to safety protocols.Key Responsibilities:Monitor project timelines for accurate patient enrollmentSupervise query resolution and data verification processesConduct required safety information flow reportingEnsure timely updates to study tracking systemsProvide training and mentorship to project team membersRequirements:Relevant degree in Life Sciences or equivalentMinimum 4 years of clinical monitoring experienceKnowledge of CAR-T and GI therapies preferredStrong communication and problem-solving skillsAbility to travel extensively based on project demandsBring your clinical research expertise to PSI and contribute to impactful therapeutic developments.#J-18808-Ljbffr

📌 Clinical Research Associate With Psi (Toronto)
🏢 PSI
📍 Toronto