PSI CRO

Compensation

Full Description

Company Description PSI is a leading Contract Research Organization with more than 29 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. Job Description Line manages assigned departmental staff (Clinical Research Associates) Interacts with other PSI departments on issues resolution and joint initiatives Conducts performance appraisal and fosters professional development of departmental staff Administratively supervises departmental staff Manages resource allocation to projects and resolution of resourcing conflicts, resource workload and utilization, as well as staff performance to ensure efficiency and productivity Provides mentorship to department staff Plans training and tracks its completion for the assigned department staff Develops and implements quality systems, including quality systems documents (shared responsibility with Senior Clinical Operations Manager and Associate Director Clinical Operations) Implements quality controls within the department Prepares for and participates in site and systems audits/ regulatory inspections Performs supervised monitoring visits (shared responsibility with Associate Director Clinical Operations) Oversees planning, conduct and reporting of field training (shared responsibility with Associate Director Clinical Operations) Participates in Risk Review Meetings and CAPA investigation meetings Manages crisis and resolves conflicts on project and trial site levels Attends project review meetings with the local project teams Participates in project-specific site identification and selection Ensures enrollment in ongoing projects and communication with sites Participates in feasibility assessment of potential and ongoing projects Assists with Business Development tasks such as client meetings, trade fairs, key medical events and networking with medical communities and opinion leaders Qualifications MD, PharmD or university degree in Life Sciences At least 5 years’ industry experience in clinical research with verified relevant experience in line management Previous line manager experience Previous experience as a Clinical Research Associate/Monitor Candidates based in Pacific Time Zone strongly preferred Additional Information 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.