Manager, Clinical Monitoring

Precision for Medicine is growing! We are hiring a Manager, Clinical Monitoring based in Italy. The position can be fully remote. Position Summary : The Manager of Clinical Monitoring (GCM) provides a development pathway for clinical research professionals. Responsibilities include managing and developing the organization’s Clinical Research Associate (CRA) workforce and supporting departmental initiatives to improve quality and productivity. This role requires the ability to independently lead, manage, and motivate a team of CRAs (employees and/or consultants) to uphold Precision for Medicine’s standards and focus on quality. The manager will ensure proper resource allocation, provide career development support, and aim to minimize turnover while maintaining high employee satisfaction. Essential functions include but are not limited to : Develop action plans and oversee strategies to optimize CRA services, focusing on high-quality delivery of goals. Assist in project resourcing, ensuring appropriate resource allocation and updating tracking systems. Collaborate with Clinical Team Leads / Clinical Trial Managers to meet resource and site requirements. Develop, mentor, manage, and coach CRA staff to meet quality standards and support career growth. Conduct site visits to assess CRA skills and address project-specific issues. Identify quality risks, recommend corrective actions, and address performance issues. Ensure staff have necessary resources, training, and system access. Maintain accurate administrative updates and reports. Work with the Clinical Operations Team to improve CRA procedures and efficiency. Develop metrics for CRA oversight and participate in their evaluation. Participate in interviewing and onboarding new CRA staff. Represent the company professionally and manage staff in alignment with company policies. Perform additional duties as assigned by leadership. Qualifications : Degree in a scientific or healthcare discipline or equivalent experience. Minimum 7 years in clinical operations or related fields, with at least 5 years onsite monitoring experience, including electronic and paper medical records. Strong monitoring experience in oncological clinical trials. 3-5 years of direct supervisory experience managing CRAs, including developing training programs and evaluation processes. Willingness to travel domestically and internationally (~25%). Skills and Competencies : Mastery of ICH-GCP, local regulations, SOPs, and clinical study phases. High emotional intelligence and passion for people management. Ability to develop training plans and hold personnel accountable. Deep understanding of clinical research operations and problem-solving at the site level. Experience with EMRs and EDCs. Self-motivated, organized, and proactive in improving processes. Professionalism in punctuality, commitments, and interpersonal interactions. Proficiency in delivering formal presentations to diverse audiences. We comply with privacy policies and are an Equal Opportunity Employer. For accommodations or concerns about fraudulent job offers, contact us at [email]. J-18808-Ljbffr

Location: puglia, IT

Posted Date: 5/9/2025