FIND_THE_RIGHTJOB.
Dallas, United States
POSITION RESPONSIBILITIES:
· Being one of a team of Clinical Research Coordinators conducting clinical research trials in the ophthalmology (retina) field.
· Conduct testing that includes:
o Imaging (ZEISS, Heidelberg OCT’s, OPTOS, and Fundus Photography)
o Refraction and Visual Acuity Examinations
o Vital Signs
o Visual Fields
o Electrophysiology
· Completion and maintenance of regulatory and study start-up documentation
· Maintenance of investigator site files
· Collection, documentation, and filing of clinical research data, including patient medical records.
· Assess potential subject eligibility based on specific inclusion/exclusion criteria.
· Adheres to good clinical practice (GCP), OSHA, and HIPAA guidelines.
· Scheduling and tracking of patient appointments.
· Administering and explaining consent forms and questionnaires to patients with low vision.
· Process and ship biological specimens for studies.
· Submission of data to reading centers and EDCs
· Works collaboratively with the investigators, study team, IRB, Sponsors, and study monitors.
· Works well under deadlines.
· Enjoys working with a wide range of population of patients.
QUALIFICATIONS
· Bachelor’s Degree required from an accredited institution. The field of science is a plus.
· CCRC, CCRP, COA, or equivalent knowledge, a plus.
· Preferred experience in Ophthalmology.
· Phlebotomy experience a plus.
· An expressed interest in Clinical Research with a willingness to learn.
· High attention to detail and problem-solving skills required.
· Data quality and work ethic of the highest standard.
· Strong interpersonal, writing, and communication skills required.
· Work independently with minimal supervision, and enjoys working as part of a team.
· Ability to effectively operate the following software programs: Windows, Microsoft Word, and Excel.
Job Type: Full-time
Pay: $55,000.00 - $75,000.00 per year
Benefits:
Work Location: In person
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