Clinical Study Operations Manager

To ensure the successful operational delivery of clinical studies, the full-time Clinical Study Operations Manager will oversee study startup planning, site onboarding, and ongoing operational oversight while working remotely across the U.S. with up to 10% travel required. Key responsibilities Collaborate with project teams to implement study startup activities, including communication planning and logistics Act as the primary point of contact for clinical sites, ensuring smooth operations and clear communication Monitor project progress to ensure adherence to timelines, protocols, and quality standards Required qualifications 5+ years of experience in clinical project management or clinical operations roles Familiarity with GCP, ICH guidelines, and clinical research regulatory requirements Strong organizational and project management skills Proactive mindset with the ability to identify priorities and anticipate challenges Desire to learn more about analytics, statistics, machine learning, and clinical trials