Senior Clinical Project Manager

Position Overview:

• Responsible for overseeing and managing trials within clinical programs.
• Includes management and oversight of CROs and other service providers.
• Responsible for planning, organizing, and directing the completion of trials on time, on budget, and within scope.

Essential Duties:

• Master the basic elements of the study protocol, investigator brochure, informed consent forms, and study specific materials
• Evaluate and qualify CRO’s/vendors/investigator sites in a systematic and organized fashion
• Lead regularly scheduled project meetings or ad-hoc discussions with an agenda for tracking meeting minutes and action items

Necessary Skills and Abilities:

• Detail oriented and organized, and adept at data entry, reporting and maintaining comprehensive records
• High level of professionalism, including meeting-presence & etiquette
• Strong communication skills (both verbal and written), able to communicate with executives and staff