Clinical Operations Lead

PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. 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. The scope of responsibilities will include: - Line manage, coach, mentor, and develop Clinical Operations staff across multiple experience levels. - Supervises and conducts training of Monitors. - Mentors Monitors. - Plans and conducts supervised monitoring visits with training, authorization, and ongoing assessment purposes.  - Supports professional development of Monitors. - Contributes to the performance appraisal of Monitors.  - Supports Clinical Operations Managers with resource allocation and utilization of departmental staff. - Performs other Clinical Operations supervisory tasks.  - MD, PharmD, or a university degree in Life Sciences - Previous clinical research industry experience is required. - Previous experience working independently as an onsite Clinical Research Associate (CRA) is required (minimum of 4 years)  - 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.