Clinical Research Coordinator

Tasks Scoped:

Recruitment:

Retention:

Administrative Tasks:

Assist with Study Visits, sample collection and processing - excluding venipuncture and study drug administration
Study visit and audit preparation - monitoring visits
Consenting
Administrative tasks - maintaining study binder, regulatory filing, etc.
Source Document Creation
Regulatory document maintenance, preparation, and submission of study level IRB/Regulatory documents from approved templates

Important Details:

Education/Experience Required: 1+ years of experience as a CRC within the Ophthalmology space, if no experience with Ophthalmology then 3+ years as a CRC is a MUST HAVE
Schedule/Shift: 40 hours per week, Monday - Friday 8AM - 5PM
Assignment Duration: 10 month contract; project wrap up estimated to be in September 2025

Benefits:

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

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

Clinical Research Coordinator