Clinical Operations Manager

PSI is seeking an experienced and people-focused Clinical Operations Manager to join our team. We’re looking for a knowledgeable, proactive, and result-oriented professional to join our management team and help lead and further develop our Clinical Operations team in Latin America region. You will lead and mentor a high-performing team while ensuring efficient resource utilization, operational excellence, and the successful delivery of clinical trials. In this role, you will enjoy a broad range of operational and strategic management responsibilities, while contributing to the continued growth and success of the region. This is a hybrid role based in Buenos Aires.  The scope of responsibilities will include: • Line manage, coach, mentor, and develop Clinical Operations staff across multiple experience levels. • Manage hiring, onboarding, performance management, and professional development activities. • Oversee resource allocation, workload planning, and utilization across clinical trials. • Collaborate with Project Managers and cross-functional teams to ensure successful study delivery. • Monitor staff performance and support operational efficiency through established departmental metrics. • Implement departmental quality controls and contribute to the development and continuous improvement of quality systems and processes. • Prepare for and participate in internal audits, sponsor audits, and regulatory inspections. • Support trial execution by resolving operational challenges and facilitating communication between project teams and investigational sites. • Participate in feasibility assessments for new and ongoing studies. • Support business development activities, including client meetings, networking events, and operational discussions, as needed. • MD, PharmD, or a university degree in Life Sciences • Minimum of 5 years of clinical research industry experience, including demonstrated team management or people leadership experience. • Previous experience working independently as an onsite Clinical Research Associate (CRA) is required. • Previous experience managing or mentoring clinical research professionals in a CRO, sponsor, or related clinical research environment. • Previous experience with Oncology or IBD is a plus. • Strong leadership, coaching, and employee development skills. • Experience with resource planning, workload management, and performance management. • Working knowledge of ICH-GCP, applicable regulatory requirements, and clinical trial operations. • Experience supporting audits, inspections, and quality initiatives is preferred. • Excellent communication, organizational, and problem-solving skills. • Proficiency with Microsoft Office applications and clinical research systems. • Advanced English proficiency (written and spoken). • Strong interpersonal skills with the ability to build trust, foster collaboration, and develop high-performing teams. Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.