Clinical Research Coordinator

Posted 2 Days Ago
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San Antonio, TX, USA
In-Office
Junior
Healthtech
The Role
Coordinates and administers multiple ophthalmic clinical trials, including patient visits, informed consent, data collection, case report forms, adverse-event reporting, study medication, specimen processing, protocol compliance, sponsor monitoring visits, and ophthalmic imaging. Provides patient support, maintains accurate records, protects health information, and follows FDA, HIPAA, OSHA, and research protocol requirements.
Summary Generated by Built In
Company Overview

Medical Center Ophthalmology Associates located in San Antonio Texas offers compassionate care for every eye condition.(MCOA) Board certified physician's offer comprehensive eyecare their team is totally dedicated to help you see better.

Position Summary

Medical Center Ophthalmology Associates (MCOA), in San Antonio, TX, is now hiring an enthusiastic Clinical Research Coordinator to join our growing team. The Clinical Research Coordinator is responsible for the coordination and administration of clinical trials under the direction of the Clinical Research Manager, the Principal Investigator, and the Research Director. The team member will implement and coordinate research and administrative procedures for the successful management of clinical trials. 

Responsibilities

A CRC is responsible for performing procedures and coordinating the execution of clinical trials in accordance with research protocols.


  • Administratively and clinically manage 5-7 concurrently running clinical research trials, including data collection, data query response, and issue resolution within a timely manner. 
  • Identify adverse events and report per protocol guidelines. 
  • Assist in the planning and design of source documents for study protocols. 
  • Conduct pre-study, initiation, monitoring, and close-out visits with sponsor representatives.  
  • Provide patient care, not limited to but including greeting patients in a friendly and prompt manner, responding within appropriate time frame to patient questions and communications, escorting patients to exam rooms, verifying patient information, making necessary documentation within patient charts, discussing study protocols with patients, and ensuring correct informed consent is documented.   
  • Work closely with physicians and doctors to update on changes in patient’s health.  
  • Administer topical ophthalmic or oral medications. 
  • Maintain knowledge of operation and maintenance of clinical equipment, drugs, and supplies.  
  • Discuss study protocols with patients and verify the informed consent documentation 
  • Dispense study medication in a professional and accountable manner following protocol requirements 
  • Collect, process, and ship blood/urine specimens at scheduled patient visits 
  • Schedule all patient research visits and procedures consistent with protocol  requirements 
  • Complete and maintain case report forms per FDA guidelines, and review them against  the patient’s medical record for completeness and accuracy 
  • Administer questionnaires/diaries per protocol. 
  • Maintain HIPAA compliance for all patient information. 
  • Adhere to all OSHA and Infectious Waste procedures. 
  • Obtain reading center certification and perform ophthalmic imaging and special testing when applicable 
  • Other duties as assigned. 
Qualifications

Education and/or Work Experience Requirements:


Education and/or Work Experience Requirements:

• 2+ years in healthcare, preferably ophthalmology, but not necessarily in clinical research• Analytical mindset• Attention to detail• Exceptional interpersonal skills• Superior verbal and written communication skills• Understanding of laboratory procedures and equipment• Proficiency in MS Office – Word, Excel and Outlook• High school diploma or equivalent GED


Company Benefits

We offer a competitive benefits package to our employees:

  • Medical
  • Dental
  • Vision
  • 401k w/ Match
  • HSA/FSA
  • Telemedicine
  • Generous PTO Package

We also offer the following benefits for FREE:

  • Employee Discounts and Perks
  • Employee Assistance Program
  • Group Life/AD&D
  • Short Term Disability Insurance
  • Long Term Disability Insurance

EyeSouth Partners is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Skills Required

  • At least 2 years of healthcare experience
  • High school diploma or equivalent GED
  • Analytical mindset
  • Attention to detail
  • Exceptional interpersonal skills
  • Superior verbal and written communication skills
  • Understanding of laboratory procedures and equipment
  • Proficiency in Microsoft Office, including Word, Excel, and Outlook
  • Ophthalmology experience
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The Company
1,000 Employees
Year Founded: 2017

What We Do

EyeSouth Partners is a U.S. network of integrated ophthalmology practices headquartered in Atlanta, Georgia. It supports affiliated practices with operational expertise, investments in support staff, ongoing education, and state-of-the-art technology. The network provides medical and surgical eye care through more than 70 practice affiliations, over 400 doctors, and 285 locations, including surgery centers across numerous states, serving patients with comprehensive vision-care needs.

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