Description

Summary

Coordinates all study-related and regulatory processes for the Tulane Cancer Center Office of Clinical Research (TCC OCR) and affiliate sites under the overall direction of the Director of the Clinical Research Office. Responsible for coordinating current and future Oncology research projects. Responsible for data collection and management and compliance with federal and IRB regulatory policies.

Required Knowledge, Skills, and Abilities

1. Excellent written and verbal communication.

2. Excellent computer literacy skills, including knowledge of standard office software.

Required Education and/or Experience

1. Bachelor's Degree or RN with current LA licensure at the time of hire.

2. Two years clinical research experience.

Preferred Qualifications

1. Master's degree in Public Health, Business or Social work preferred.