Job Description Summary

This position's primary function is to facilitate, promote, and ensure good clinical practice in the conduct of all research protocols in the Department/Center. Independently manages different phases of complex clinical trials and mentors Coordinators and Research Assistants. Works with partnering institutions and creates multi-center budgets and manages expenses. Participates in study team meetings, disease site group meetings, and ongoing protocol training/compliance meetings. Supports in the monitoring of external sites and assists in the management of multisite trials. Adheres to all University and other regulatory guidelines.

Job Description

This position is contingent upon favorable funding.

Assists in clinical research tasks related to Cardiology. A variety of skills will be utilized, including: screening subject records for eligibility, recruitment and consenting of study subjects, data entry, database management, coordinating with study team members and other external department members, performing study related diagnostic testing, coordinating research studies, and processing and shipping samples. The candidate must be organized, detail oriented, accountable, and adaptable.

Qualifications

Bachelor's Degree with 2-4 years of related experience in research and clinical study methodologies or equivalent combination of education and experience is required

Working Conditions

Office, Library, Computer Room; Requires extensive safety

Physical Effort

Typically sitting at a desk or table; Occasional lifting 25 lb. or less