Clinical Research Coordinator

Eye Associates of New Mexico has an outstanding career opportunity in our Vision Research Department.

Eye Associates of New Mexico is the largest Ophthalmology and Optometry practice in the Southwest. We serve our communities with compassionate, state-of-the-art and valued based care. Our team approach aims to deliver the highest quality eye care to all. We take pride in giving the absolute highest level of patient care provided by our employees and we strive to support their professional development. 


We are currently looking for a full-time Clinical Research Coordinator. Come be a part our team and help make a difference in our patients' vision.

Some Job Duties May Include:

• Involved in department-specific clinical studies and maintains subject records                                            
• Attends investigator/coordinator meetings as required by study sponsor and Vision Research Center meetings                                            
• Assists the PI and/or Site Director in the feasibility of clinical research protocols                                            
• Assists in preparing for pre-study site visits and site initiation visits                                             
• Reads and understands the protocol and becomes familiar with study inclusion/exclusion criteria                                            
• Under the direction of the PI, performs study related procedures per the protocol visit schedule and refers to PI, Sub-I, Clinical                                             
  Research Site Director and/or Senior CRC for any study related or patient related questions. 
• Maintains HIPAA compliance    
• Accountable for test articles                                
• Ensures each candidate has completed all study related procedures 
• Participates in the collection and review of medical history and concomitant medications    
• Enters data for specific visit and transmits data/logs
• Plans and carries out programs for the recruitment, screening, enrollment, and retention of clinical research subjects and/or volunteers

Skills/ Requirements:

• Must have prior clinical research coordinator experience  
• Priority will be given to ACRP Certified Clinical Research Coordinators vs. Non-Certified Coordinators. 
• Minimum of 3 years’ experience
• Must demonstrate accurate typing skills at a minimum of 35 words per minutes

Generous Benefits:

• Paid Time Off (PTO) 
• Eight (8) Company Paid Holidays 
• Medical and Dental 
• Generous Vision Benefits 
• Flexible Spending Accounts 
• Company Paid Life and AD&D Insurance, Short Term and Long Term Disability Insurance 
• Voluntary Supplemental Life and AD&D Insurance Employee 
• Assistance Program 
• 401(k) and Roth
• Financial Wellness program
• and much more 

Eye Associates of NM is a safe team oriented culture supporting a drug-free work environment. 

To learn more about this position and our organization, please visit www.eyenm.com
 
AA/EOE/Disability. Eye Associates of New Mexico is a drug and tobacco-free employer. 

Req.# 2743