Clinical Project Manager
November 4
Description
•The Clinical Project Manager is responsible for the ownership, accountability, and results of clinical trials. •They provide project management and leadership to plan, prepare, and execute clinical studies. •The Clinical Project Manager interfaces with team members and acts as a liaison with external vendors. •Accountable for timeline development, communication, study outcomes, and delivery of trials. •Implement, manage, and terminate clinical studies per Protocols, Good Clinical Practices, and regulations. •Develop detailed plans, prioritize tasks, and oversee all elements of the clinical trial(s). •Communicate status and progress of clinical trials, addressing issues with study conduct. •Provide oversight of project team members, ensuring project-specific training is provided. •Lead development and distribution of study-specific documents. •Demonstrate knowledge of and supervise others in clinical research conduct and compliance.
Requirements
•Bachelors or master’s degree within life sciences or related field. •5+ years clinical research experience including previous monitoring experience. •Prior experience (3+ years) in the planning, conduct and management of clinical trials, with strong preference given to ophthalmic device experience. •Demonstrated ability to drive project related activities. •Previous experience leading, managing, and coaching direct reports. •Current ICH GCP certification.
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