Elevate your clinical research career with PSI as a Lead Clinical Research Associate. Manage site monitoring and protocols effectively, ensuring data integrity and compliance.PSI, a renowned Contract Research Organization, seeks a skilled Lead Clinical Research Associate. This role demands a strong background in clinical monitoring, particularly in Oncology and innovative therapies like CAR-T. You will coordinate site feasibility, monitor timelines, implement corrective measures, and ensure adherence to compliance regulations.Key Responsibilities:Coordinate investigator/site feasibility and study startup processesMonitor project timelines and patient enrollment for accuracyReview monitoring visit reports for compliance and consistencyManage query resolution and Central Monitoring observationsConduct training for site Investigators and newly promoted Lead CRAsRequirements:Minimum 4 years of site monitoring experienceKnowledge of US and Canadian regulatory guidelinesStrong background in Oncology and cutting-edge therapies preferredFull working proficiency in EnglishAbility to travel up to 65% as neededUtilize your expertise in clinical research to drive project success and ensure high standards at PSI.#J-18808-Ljbffr

📌 Lead Clinical Research Associate At Psi (Toronto)
🏢 PSI CRO
📍 Toronto