• Conduct Phase I - IV clinical research trials in indications such as skin cancer, psoriasis, acne, hyperhidrosis, rosacea and eczema. • Preparation, organization and management of clinical essential document files. • Maintain study documents in compliance with all applicable regulations. • Provide protocol specific training to ancillary research site staff. • Collaborate with the regulatory liaison to ensure all regulatory and IRB documentation is in adherence to FDA Regulations and ICH/GCP Guidelines. • Conduct study review with sponsor at site qualification, initiation, interim monitoring visits. • Assist fellow coordinators with study-related tasks, as needed. • Maintain multidisciplinary project knowledge. • Attend weekly staff meetings and review protocol specific training.

-Conduct Phase I, II & III clinical trials under Principle Investigator Supervision -Screen and enroll eligible patients into clinical trials -Maintain shadow charts containing study specific source documents -Ensure protocol compliance -Process biological specimen -Budgets, contracts and invoicing