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 Qualification 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: Open to either full time (40 hours a week) or part time (20 hours a week) employment. Work schedule would be M-F, between 8-5

Benefits (full time only):

• Paid Sick Leave (Medix provides paid sick leave according to state and local sick leave ordinances)
• Health Benefits / Dental / Vision (Medix Offers 6 different health plans: 3 Major Medical Plans, 2 Fixed Indemnity Plans (Standard and Preferred), and 1 Minimum Essential Coverage (MEC) Plan. Eligibility for health benefits is based on verifying that an average of 30 hours per week during the first 4 weeks of the work assignment has been met. If you meet eligibility requirements and take action to enroll, you will be covered no earlier than 60 days into your assignment, depending on plan selection(s).)
• 401k (eligible on the first 401k open enrollment date following 6 consecutive months on assignment. 401k Open Enrollment dates are 1/1, 4/1, 7/1, and 10/1)
• Short Term Disability Insurance
• Term Life Insurance Plan