Ophthalmic Research Coordinator, OR
Company: The Eye Group
Location: Central Point
Posted on: February 21, 2021
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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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