Clinical Team Lead

Join us in redefining what it means to work for a CRO. When you work at Rho, it’s more than just a job—you become part of the Rho Factor. We’re a proud bunch of science nerds who love tackling big challenges together. We’re not your typical CRO, and we’re not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at the heart of everything we do. Whether you’re a data wizard, analytical genius, project mastermind, or any other role, you’ll fit right into the equation of the Rho Factor. Expect plenty of geeky jokes, eccentric personalities, spontaneous brainstorms, and a supportive community where people genuinely care about their work—and each other. You’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career. We are currently hiring a Clinical Team Lead to join our team! As Clinical Team Lead II, you are integral in driving clinical research project success. You will have the opportunity to independently manage and maintain ownership of the clinical operations portion of assigned projects. You’ll provide direction to and training CRAs assigned to those projects. In addition, you will oversee of all operational aspects related to the planning and oversight of CRA and site performance as well as ensuring that sites and CRAs operate in compliance with study protocols, ICH/GCP guidelines, and Federal Regulations. Our Clinical Operations Team will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group! This role can be remote anywhere in the US. What You'll Be Doing: Proactively drive project success, including working closely with cross-functional study leadership to develop and implement operational strategies Identify and mitigate clinical risks, as well as contribute to the development of the quality risk management plan Provide skilled review of study protocols and other study materials (e.g. CRF) Develop and manage clinical operations timelines, metrics, resourcing, budget and activities Develop monitoring tools and plans Accountable for operational aspects of planning and oversight of site performance in accordance with departmental productivity expectations Create and conduct training sessions including investigator meetings, conferences, and team trainings Determine and drive the study start up process (track and report progress, review data), ensuring that all sites are selected and supplies provided in accordance with study expectations Provide status updates to project management and sponsors Lead regular clinical team teleconferences Work effectively with Site staff, as needed, serving as an escalation point for CRAs as issues arise Manage clinical Site communication and documentation of decisions, including mass correspondence to sites regarding study updates Participate in the RFP process, including internal and external business development meetings Review monitoring visit reports and ensure finalization is within contractual timeline May assist Project Managers with project management tasks as assigned Support the management and development of In-house CRAs and CRAs