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Science & Research
Clinical Research Coordinator
Humble, TX
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Overview Retina Consultants of Texas (RCTX) is seeking an individual who will be responsible to providingaccurate documentation and summarization of the ocular examination and recommendations whilemaintaining patient flow and communication regarding appointment status within a high volumepractice. Candidate will work exclusively within the EMR system (Nextech) supporting the providersas they interact with the patient. Candidate must be able to travel to multiple clinics to meet the needs of the patients andproviders, and support the clinic's variable hours (Monday - Friday, 6:30 am to 6:30pm). Schedules are provided weekly and are based on the physician's clinic, patient and surgeryschedules. Clinic staff are also provided the opportunity for weekend hours if available. RCTX offers the following competitive benefits for full-time eligible employees after theintroductory period: Medical Insurance Plans Vision Insurance Plan Dental Insurance Plan 401K Contribution Life Insurance PTO and Holiday Pay Employee Assistance Program Incentive Rewards Program Certification Opportunities Retina Consultants of Texas (RCTX) is one of the largest and most respected retina-onlyophthalmology practices in the United States, committed to Preserving the Patient's Vision. RCTXhas 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 physiciansare board certified by the American Board of Ophthalmology and specialize exclusively in diseasesand 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 mostrenowned 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 largestnetwork of leading retina specialists with the mission of saving sight and improving patient livesthrough innovation and the highest quality care. Through RCA's physician-centered practicemanagement model, physicians continue to drive clinical and practice culture while benefitting fromthe available business expertise, resources and shared best practices. Retina Consultants of Texas follows all CDC and local authority protocols to ensure the safety andwell-being of the patients, providers, employees and communities. Retina Consultants of Texas is proud to be an Equal Employment Opportunity and an AffirmativeAction Employer. We are committed to creating an inclusive work environment that celebratesdiversity. Responsibilities The Clinical Research Technician is a dual-role position responsible for providing clinicalsupport and research coordination services. This position combines ophthalmic technical skillswith research administration capabilities, requiring strong communication abilities to educatepatients about complex clinical trials and assist with informed consent processes. Thetechnician maintains patient flow, supports clinical procedures, and ensures compliance withresearch protocols while exemplifying our core values of hard work, authentic care, andinnovation.
Duties and Responsibilities:
Clinical Functions:
Obtains comprehensive patient history including chief complaint, history of present illness, patientand family history of both ocular and general illnesses, history of allergies, and current medications
Accurately performs and documents visual acuity, confrontational visual fields, evaluation of motility,pupillary function tests, dilation, and ocular tonometry
Assists physicians with laser procedures, injections, and minor procedures while maintaining sterileand safe environment protocols
Performs intraocular pressure checks after injections
Provides compassionate patient care throughout the clinic flow
Maintains cleanliness in exam and procedure rooms and back-up levels of supply stock
Counsels, consents, sets up and assists with in-office procedures
Research Functions:
Counsels and educates patients regarding clinical trials, articulating complex study informationclearly
Conducts informed consent processes for research studies
Administers all mandatory questionnaires to study subjects
Prepares visit-specific documentation and charts for Physician Clinic Team
Promptly requests all necessary medical records for Serious Adverse Event Reporting
Processes and ships laboratory biological samples for analysis
Coordinates and schedules subject visits within study/subject specific windows per protocolguidelines
Transcribes subject study information from source documents to Electronic Case Report Forms
Obtains any applicable additional/required sponsor training and/or certifications
Performs other duties as assigned
Qualifications Education Requirements:
High school diploma required
Bachelor of Science/Biology preferred
Experience Requirements:
Previous healthcare or research experience preferred but not required
Ability to understand and articulate complex concepts