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Ophthalmic Research Coordinator, OR

Company: The Eye Group
Location: Central Point
Posted on: February 21, 2021

Job Description:

Facilitate and coordinates daily clinical trial activities & all patient visits for the clinical studies Review study protocols & collect documents needed to initiate the study for sponsor submission Responsible for multiple simultaneous research studies Routinely implements, manages, and records all phases of study protocol including: Ensure compliance with protocol guidelines and requirements of regulatory agencies Establish record keeping systems Organize files including regulatory binders, study specific source documentation and other materials Create source documents for data capture per study protocol and manual of procedures Prepare and submit Initial IRB Submission documents Screen candidates for eligibility Conduct and participate in informed consent process Obtains appropriate signatures and dates on all forms for research SOP Register participants in electronic data capture for appropriate billing to funding source Collect data required by the protocol and assure timely completion of Case Report Forms Perform ETDRS refractions & visual acuity exams Collect and process biological specimen per protocol Analyze, investigate, and report adverse events Resolves queries from Sponsor in a timely manner Evaluate all lab and clinical assessments to ensure they are completed in a timely manner Maintain adequate inventory for study supplies Follow sponsor and study protocols on Investigative Drug/Device Accountability Document and supervise training and signatures of study staff on study specific training log Maintain CVs and training materials per protocol Coordinates monitor site visits and assists with preparation of site visit documentation Organize monthly research meetings with staff and physicians Attend teleconferences and Investigator Meetings Participate in recruiting eligible candidates to meet enrollment goals Job Skills & Education: Knowledge and experience in clinical trials required (Ophthalmology preferred) Certified Clinical Research Coordinator or Professional (CCRC/CCRP) is preferred Certified Ophthalmic Assistant or Certified Ophthalmic Technician is preferred Proficiency in Microsoft Office (Word, Excel) Ability to perform venipuncture & experience with processing of lab specimens Proficiency in performing ETDRS refractions and visual acuity exams Excellent organizational skills and attention to detail is required Ability to prioritize & multi-task Must be self motivated and take initiative Excellent teamwork attitude is required

Keywords: The Eye Group, Medford , Ophthalmic Research Coordinator, OR, Other , Central Point, Oregon

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