What are the responsibilities and job description for the Ophthalmic Technician/Clinical Research Coordinator position at Global Research Management, Inc.?
ESSENTIAL FUNCTION OF THE OPHTHALMIC TECHNICIAN / CLINICAL RESEARCH COORDINATOR :
Responsible for the oversight, execution, and successful completion of study protocols
Operates and upholds Good Clinical Practice (GCP) and Company Standard Operating Procedures (SOPs).
Coordinates with all departments and team members to streamline operations and ensure the successful execution of patient study visits with quality and accurate data.
RESPONSIBILITIES INCLUDE (but not limited to) :
Review and understand the protocol, Inclusion / Exclusion criteria, procedure manual, and eCRF guidelines for each clinical trial they are assigned to.
Actively seeks to identify potential subjects from our database to prescreen and enroll in ongoing studies.
Responsible for completing study specific assessments, and monitoring participants test results, including but not limited to Adverse Events, lab results, vitals, ECG, and other study procedures (escalating any protocol or safety concerns to the appropriate medical group and management.)
Attends Site Initiation Visits, Investigator meetings (as requested), bi-weekly staff meetings, monitoring visits, and any other meetings that may arise.
Responsible for overseeing all study subjects according to protocol specific requirements and GCP guidelines.
Ensure lab and medical results are completed, and all eligibility requirements are met.
Ensure quality assurance (QA) is performed on all electronic and paper source documents.
Performs other related work as required and assigned by practice administrator or direct supervisor.
REQUIREMENTS / EXPERIENCE :
Bilingual English and Spanish
Minimum of 1 year of experience as an Ophthalmic Tehcnician
Experience in : IOP, visual acuity, manifest refraction, fundus photography, OCT photography (preferred knowledge in Heidelberg), visual field, scribing, schirmers, corneal staining, pachymetry
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