Clinical Project Manager

As a Clinical Project Manager, you will be responsible for overseeing clinical trials with a focus on interventional studies (Phase IIV). Your key responsibilities will include: - Directly managing and operationalizing clinical trial protocols into eSource/EDC workflows. - Managing end-to-end clinical trial processes such as start-up, site initiation, data collection, query management, and close-out. - Leading and mentoring CDM/clinical trial teams with a minimum of 5 years of people management experience. - Utilizing expertise in clinical trial systems like CTMS (CRIO preferred), eSource, and EDC platforms. - Working in pharmaceutical, biotechnology, or CRO environments across various therapeutic areas. - Ensuring compliance with regulatory requirements such as ICH-GCP, FDA, EMA, and HIPAA. - Handling system validation, change control, and maintaining audit/inspection readiness. You should have 10-15 years of experience in clinical trials, a strong background in managing interventional studies, and a thorough understanding of regulatory standards. Your experience in people management and expertise in clinical trial systems will be essential for success in this role.,