Leveraging your hands-on clinical research experience and deep understanding of site operations, you will assess site workflows, identify opportunities for operational improvement, and deliver tailored training and support that promote research best practices, accelerate clinical trial execution, and drive adoption of Iterative Health's services and technology. Hands-on experience supporting Phase II–IV pharmaceutical-sponsored clinical trials, including study start-up, confidentiality agreements (CDAs), feasibility assessments, regulatory documentation, SOPs, study protocols, and applicable clinical research regulations.