Clinical Research Coordinator

Eye Associates Of New Mexico•Albuquerque, NM

8d•Onsite

About The Position

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 value-based care. Our team approach aims to deliver the highest quality eye care to all. We take pride in providing the absolute highest level of patient care through our employees, and we strive to support their professional development. We are currently looking for a full-time Clinical Research Coordinator, to join our Vision Research team. If you are detail-oriented, passionate about advancing patient care through clinical research, and enjoy working in a collaborative healthcare environment, we encourage you to apply. Come be a part of our team and help make a difference in our patients' vision.

Requirements

Prior clinical research experience or Certified Clinical Research Coordinator (CCRC) certification preferred
Strong attention to detail with accurate data entry skills
Experience working within sponsor electronic data systems is preferred
Ability to maintain screening and recruitment logs using Excel or Microsoft Word
Strong organizational, communication, and critical thinking skills
Phlebotomy experience preferred
Ophthalmology experience or COA, COT, or COMT certification is a plus, but not required

Responsibilities

Coordinate clinical research studies under the direction of the Principal Investigator and Vision Research leadership
Maintain accurate study documentation, subject records, and source documents
Perform study-related procedures in accordance with research protocols, Good Clinical Practice (GCP), ICH, and FDA guidelines
Screen, recruit, enroll, and retain study participants while ensuring protocol compliance
Collect medical histories, concomitant medications, and study-specific clinical data
Enter and maintain study data within sponsor electronic data capture (EDC) systems
Prepare for sponsor site visits, audits, and regulatory inspections
Assist with Institutional Review Board (IRB) submissions and regulatory documentation
Coordinate specimen collection, processing, storage, and shipment as required
Communicate with physicians, study sponsors, regulatory agencies, and research participants
Support adverse event documentation and follow-up
Maintain HIPAA compliance and ensure confidentiality of research participants
Assist with scheduling research visits and providing ongoing patient education