As a clinical research coordinator, Proficient in coordinating all phases of clinical trials, including protocol review, regulatory compliance, and site management.Also Proficient in data collection, entry, and management. Ensure accuracy and completeness of study data while adhering to SOP .
- Mon – Fri: 09:00AM – 06:00PM
- 1236 Poydras St, Ste - 301A, New Orleans, LA 70113
- (+1) 504-420-7800