Clinical Project Manager

• Plan and execute operational aspects of a research project utilizing MS Project;
• Develop and monitor project timelines and budgets;
• Assign project staff resources and oversee completion of tasks;
• Assist in development of protocol and case report forms;
• Manage the development of study manual of operations and perform site visits as needed;
• Oversee site management, recruitment, enrollment, and data collection for research studies;
• Interface with study sponsors, contractors and vendors;
• Provide oversight of periodic reporting to regulatory agencies and sponsors.

Qualifications:

• BA/BS/MA/MPH plus 3-5 years of direct research project management experience. PMP certification is desirable, but not required;
• Ability to manage and direct 1 or more research projects, including management of study budgets;
• Must possess full working knowledge of all required study tasks and elements from study initiation through completion. High level of working knowledge with GCP, ICH and FDA regulations on clinical research projects are helpful, but not required;
• Excellent oral and written (including email correspondence) communication skills;
• Ability to supervise and mentor junior staff members;

Proficiency with Microsoft Office products, including MS Project