Project Coordinator- School of Medicine, OBGYN Oncology

Emory University•Atlanta, GA

13d•Hybrid

About The Position

Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. We welcome candidates who can contribute to the excellence of our academic community. This role manages multiple projects concurrently, ensuring priorities, timelines, and deliverables are effectively coordinated and achieved. It also coordinates the strategic planning process, assists in developing and monitoring project-related budgets and tasks, and coordinates logistical arrangements for conferences, conventions, or meetings. The position may involve identifying funding resources, developing funding strategies, and writing grants or other promotional materials. Additionally, it includes clinical data entry, administering patient surveys, database management, and cross-training in research activities. The role also provides operational support to other clinical research coordinators to ensure efficient study conduct and compliance.

Requirements

A bachelor's degree in a related field and three years of related project management experience, or an equivalent combination of experience, education and training.

Responsibilities

Manages multiple projects concurrently ensuring priorities, timelines and deliverables are effectively coordinated and achieved.
Coordinates the strategic planning process and monitors progress toward achieving project goals.
Assists in developing, administering and monitoring project related budgets.
Coordinates logistical arrangements for related conferences, conventions or meetings.
May assist in identifying funding resources and in developing funding strategies and initiatives.
Develops and generates various operational and statistical reports.
Represents and promotes the project at various speaking engagements.
May write grants, reports, briefings, newsletters, promotional or other written material related to the project.
Performs related responsibilities as required.
Clinical data entry
Administering patient surveys
Database management
Cross-training in research activities to build additional skills over time
Assists and provides operational support to other clinical research coordinators in the coordination and management of clinical trials to promote efficient study conduct and compliance with applicable protocols and regulatory requirements.
Assists in developing, administering and monitoring project related tasks.
Develops and generates various operational and study reports.
Represents and promotes the project at various speaking engagements/meetings.
May write grants, reports, briefings, newsletters, promotional or other written material related to core projects.