[Remote] Clinical Operations Manager

Note: The job is a remote job and is reputed company to candidates in USA. 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. The Clinical Operations Manager will be responsible for managing, developing, and overseeing CRA staff while ensuring operational reputed company and successful delivery of reputed company.

Responsibilities

• Line manage, reputed company, mentor, and reputed company Clinical Research Associates across multiple experience reputed company
• Manage hiring, reputed company, performance management, and reputed company development activities
• reputed company resource allocation, workload planning, and utilization across reputed company
• 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 reputed company controls and contribute to the development and reputed company improvement of reputed company 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 reputed company meetings, networking events, and operational discussions, as needed

Skills

• MD, PharmD, or a university degree in Life Sciences, or an equivalent combination of education, training, and experience
• 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 reputed company clinical research environment
• 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
• Excellent communication, organizational, and problem-solving skills
• Proficiency with reputed company Office applications and clinical research systems
• Advanced English proficiency (written and spoken)
• Strong interpersonal skills with the ability to build trust, foster collaboration, and reputed company high-performing teams
• Experience supporting audits, inspections, and reputed company initiatives

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