Clinical Research Assistant

Found in: Resume Library US A2 - 2 weeks ago

Conroe Texas, United States Retina Consultants of Texas Full time
Overview:
Retina Consultants of Texas (RCTX) is seeking a responsible individual who will be responsible for providing patient care to patients enrolled in research clinical trials.This individual should be detailed oriented. Position will be based from the Woodlands clinic.

 

Candidate must be able to work shift anytime between 6:30 am -5 pm, Monday-Friday.

 

RCTX offers the following competitive benefits for full-time eligible employees after the introductory period:

Medical Insurance Plans

Vision Insurance Plan

Dental Insurance Plan

401K Contribution

Life Insurance

PTO and Vacation Pay

Rewards and Recognition Program

Certification Opportunities

 

Retina Consultants of Texas (RCTX) is one of the largest and most respected retina-only ophthalmology practices in the United States, committed to Preserving the Patient's Vision. RCTX has three certified research centers and is home to the Greater Houston Retina Research Center, one of the country’s leading sites for retinal research. All Retina Consultants of Texas physicians are board certified by the American Board of Ophthalmology and specialize exclusively in diseases and surgery of the retina, vitreous, and macula. In addition, RCTX has an ocular oncology division, which focuses on cancer treatments for the eye. Our surgeons have studied at some of the most renowned institutions in the nation and all have graduated at the very top of their classes.

 

Retina Consultants of Texas (RCTX) is part of Retina Consultants of America (RCA), the largest network of leading retina specialists with the mission of saving sight and improving patient lives through innovation and the highest quality care. Through RCA's physician-centered practice management model, physicians continue to drive clinical and practice culture while benefiting from the available business expertise, resources and shared best practices.

 

Retina Consultants of Texas follows all CDC and local authority protocols to ensure the safety and well-being of the patients, providers, employees and communities. 

 

Retina Consultants of Texas is proud to be an Equal Employment Opportunity and an Affirmative Action Employer. We are committed to creating an inclusive work environment that celebrates diversity.

Responsibilities:
Coordinate and schedule subject visits within study/subject specific windows per protocol guidelines.

Prepare visit-specific documentation and charts for Clinical Research Coordinator

Inform subjects and obtain written consent in regard to ICF’s

Assist Coordinator in patient care and management

Assist Coordinator in monitoring subject flow and assist in subject care and management

Accurately collect and record all necessary data (e.g. demographics, medical history, adverse events, concomitant medications, etc.) during study visit

Transcribe subject study information from source documents to the Electronic Case Report Forms

Administer all mandatory questionnaires to study subjects

Set up, prepare subject, and conduct electrocardiograms on subject who require ECG per study protocol

Scribe ocular exams for doctors and confirm appropriate treatment per protocol

Promptly request all necessary medical records for Serious Adverse Event Reporting

Collection, processing, and shipment of laboratory biological samples for analysis

Perform intraocular pressure checks post-injections

Review and resolve data management queries as need

Trial frame refraction and ETDRS visual acuity testing

Other duties as assigned

Qualifications:
Skills/Competencies:

Biliginual preferred

Ability to multitask

Computer efficient

Commnucates well both verbally and electronically; email, MS Teams, etc.

Detail oriented

Education Requirements

Bachelors degree or 4 years of ophthalmic experience in lieu of degree

 Experience Requirements:

No experience required with a Bachelors degree otherwise at least 4 years of ophthalmic experience 

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