Research Clinical Assistant

Research Clinical Assistant Vitreo Retinal Consultants - 3.0 Hauppauge, NY Job Details Full-time $20 - $23 an hour 7 days ago Benefits Health insurance Dental insurance 401(k) Paid time off Vision insurance Flexible schedule Life insurance Qualifications Direct patient care Patient monitoring Medical scheduling High school diploma or GED Transcription Organizational skills Implementing research protocols Full Job Description Vitreoretinal Consultants of NY is the premier retinal care destination for patients across Long Island, Queens, NYC, and beyond. Founded in 1981, our team of nationally-recognized retina specialists and surgeons have established themselves as distinguished physicians, compassionate providers, and key thought leaders in the retina care community. We are committed to providing a compassionate and ethical environment that focuses on patient-centered care. From diagnostics to clinical trials, we bring clarity, transparency, and humanity to all aspects of what we do. We have a very high level of patient satisfaction and are proud of our reputation, online and in the medical community.

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//www.vrcny.com/why-vrc Position Summary The research assistant is primarily responsible for assisting in research patient visits according to ICH-GCP guidelines and according to the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending on individual experience/knowledge and the needs of the organization which are subject to change from time to time.

Job Description Level I Minimum Qualifications:

Education:

High School diploma or the equivalent, with significant relevant experience College Degree Preferred Experience / Knowledge /

Skills:

Effective oral and written communication Delivers safe and appropriate care to patients in addition to the requirements outlined by study protocols Adapt quickly with each new change and must be flexible with change of any system or method. Ophthalmology and/or Optometry experience preferred

Phlebotomy Experience Preferred Duties:

Coordinate and schedule subject visits within study/subject specific windows per protocol Prepare visit-specific documentation and charts for Clinical Research Coordinator Observe Coordinator in patient case and management Assist Coordinator in monitoring subject flow and assist in subject care and management Observe, assist, collect and record all necessary data for follow up (e.g. adverse events, concomitant medications, etc.) study visits (Phase 2 & 3; NO Gene Therapy) 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 (ECG) on subjects as required per study protocol Promptly request all necessary medical records for Serious Adverse Event Reporting Process and ship laboratory biological samples for analysis Perform intraocular pressure checks after injections Perform trial frame refraction and ETDRS visual acuity testing (For ISTs only, at selected sites) Inform subjects and obtain written re-consents in regard to ICF's Perform other duties as assigned Obtain any applicable additional/required sponsor training and/or certifications

Job Type:

Full-time Pay:

$20.00 - $23.00 per hour

Benefits:

401(k) Dental insurance Flexible schedule Health insurance Life insurance Paid time off Vision insurance Application Question(s): Do you have any phlebotomy experience?

Work Location:

In person