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Azul Vision · 1 day ago

Clinical Research Coordinator

Pasadena Clinic - Pasadena, CA 91107

Full-time

Onsite

Entry, Mid Level

$22/hr - $26/hr

2+ years exp

Azul Vision is a company focused on the eyecare industry, and they are seeking a Clinical Research Coordinator to assist in recruiting and managing research studies. The role involves overseeing clinical trials, ensuring compliance with protocols, and maintaining documentation related to the studies.

Health CareMedicalWellness

Responsibilities

Interpret, comprehend, and conduct clinical research procedures while following all protocols

Oversee all aspects of patients involved in clinical trials. Ensure procedures are completed properly, while taking guidance from sponsors. Follow up and keep track of patients care at all times

Pre-screen detailed chart review of potential patient records. Call referring physicians to discuss patients, follow up with patients to discuss details of the trial and take proper documentation

Manage and ensure completion of all study start-up documents for proper documentation and compliance

Discuss and review in detail the informed consent with patients and their family members to ascertain proper informed consent per GCP guidelines

Provide direction to staff and providers relative to the daily activities and tasks associated with conducting each clinical research

Train staff as necessary to ensure compliance and protocol for each trial

Prepare and ensure accurate IRB submissions, including additional review, safety, and close-out reports

Coordinate site visits with Sponsors to ensure professional representation of Azul Vision and positive sponsor experience

Oversee completion of delegation logs and delegation training for all clinical research personnel

Maintain all regulatory binders in accordance with Sponsors specifications and general industry standards

Create, implement, and maintain all clinical research related to SOP’s

Report and follow-up on all adverse events

Oversee recruitment, management, and follow-up of patients involved in clinical trials

Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries

Perform photography including OCT/ Color Fundus/ Fluorescein angiography / Visual Field / Specular Microscope

Accurately performs Snellen VA or manual refraction/ tonometry

Responsible for performing ECGs and vital signs

Perform ophthalmic and research technician duties

Other duties as assigned

Qualification

Clinical research experienceOphthalmic technician experienceEye anatomyMicrosoft Office proficiencyAnalytical skillsOrganizational skillsCommunication skillsTime management skills

Required

High School Diploma or GED required

A minimum of 2 years of experience in the clinical research industry

Prior ophthalmic technician experience is highly desired

Through knowledge of eye anatomy, disease, symptoms, and ocular medications

Exceptional organizational skills - will be expected to balance multiple tasks, respond promptly to emails, and re-prioritize tasks based on last-minute deadlines

Ability to interact with supervisory staff, physicians, peers, external customers, and patients positively, energetically, and professionally

Excellent oral and written communication skills

Proficiency in the use of Microsoft Office products

Organizational and time management skills

Working knowledge of the clinical research regulatory framework and institutional requirements

Demonstrate ability to convey ideas and information effectively

Analytical skills and good judgment