• Coordinating a clinical trials
• Planning and execution of a project
• Managing a trial from site selection, startup and enrollment to close-out
• Managing clinical research associates' productivity, Contacting investigators and internal project teams
• Developing and implementing risk management strategies and contingency plans for clinical deliverables
• Ability to complete Quality Compliance Support (Audit, product quality and adverse report handling).
• Mentoring and training of the Clinical Research Associate
• Facilitating effective communication between investigative sites, the client and sponsor
• Responding to sponsor, client and federal regulatory requirements/audits
• Product...