Clinical Project Manager

Description

• Responsible for overall delivery of clinical study;
• Main point of contact for sponsors and study teams;
• Development of study-related documents;
• Attending and presenting at investigator meetings;
• Participation in project start-up activities (i.e., protocol review and implementation, kit supply ordering, coordination of kits, lab manual and requisition production and shipping);
• Day-to-day monitoring of project status through status reports and timeline documents;
• Providing support to research sponsors and clinical sites; and
• Occasional handling of biological samples is a possibility.

Qualifications

• Minimum Bachelor's degree in science or a health-related field;
• Knowledge of Microsoft Office;
• 1 - 3 years of clinical laboratory experience; and
• MT (ASCP) certification is preferred.