Job Title: Study Coordinator - Part Time

Job Location: ONSITE - Sarasota, FL 34239

Job Description:

Are you ready to give your career a boost by bringing your talents and expertise to some of the nation's top companies? At Medix, we are dedicated to creating opportunities for talent through our Healthcare, Scientific and Information Technology divisions. Our dedicated recruiters offer a personalized service to make sure we truly understand your employment needs.

Medix is looking for a part time, contract clinical research coordinator to support opthalmology trials in the Sarasota, FL area. This contract is currently expected to have a duration through September 2025, and we are looking for someone to commit to 20 hours a week, onsite, during daytime business hours (M-F, between 8 AM - 5 PM)

Responsibilities/ Job Duties:

Contract clinical research coordinator assignment coordinating complex ophthalmology trials. Employee will assist with Study Visits, sample collection and processing - excluding venipuncture and study drug administration - audit preparation, monitoring visits, consenting, query resolution, data entry and data migration, AE monitoring, prescreening for eligibility, as well as scheduling appointments and sending appointment reminders.

Minimum Education and Experience Requirements:

• Minimum 2 years clinical trial coordination experience
• Experience with EDC data entry/management, query resolution required
• Experience with study visit management including screening, enrollment, consenting, etc. required
• Experience managing regulatory documentation including managing regulatory binders required
• Ophthalmology experience preferred
• Bachelors degree preferred

Schedule/ Shift: Part time - 20 hours a week. Site schedule is 8:30 - 4:00 PM, M-F, exact weekly schedule open to discussion

Medix is acting as an Employment Business in relation to this vacancy.