Clinical Research Assistant for Ophthalmology Clinic Position Available In Broward, Florida

Clinical Research Assistant for Ophthalmology Clinic Retina Group of Florida – 3.9

Fort Lauderdale, FL Job Details Full-time Estimated:

$37.8K – $47.5K a year 19 hours ago Benefits Health savings account Health insurance Dental insurance 401(k) Flexible spending account Paid time off Employee assistance program Vision insurance 401(k) matching Employee discount Life insurance Retirement plan Qualifications Responsible conduct of research Research ethical considerations Ophthalmology High school diploma or GED ICH guidelines Data logging Attention to detail Organizational skills Communication skills Entry level Full Job Description Job Summary We are seeking a dedicated and detail-oriented Clinical Research Assistant to join our team! The Clinical 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 upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.

Duties:

Coordinate and schedule subject visits within study/subject specific windows per protocol guidelines. Prepare visit-specific documentation and charts for Clinical Research Coordinator Observe Coordinator in patient care 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

Minimum Qualifications:

Education:

High School diploma or the equivalent, with significant relevant experience College degree preferred Ophthalmic experience 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

Job Type:

Full-time Benefits:

401(k) 401(k) matching Dental insurance Employee assistance program Employee discount Flexible spending account Health insurance Health savings account Life insurance Paid time off Retirement plan Vision insurance

Physical Setting:

Clinic Ability to

Commute:

Fort Lauderdale, FL 33308 (Preferred) Ability to

Relocate:

Fort Lauderdale, FL 33308: Relocate before starting work (Preferred)

Work Location:

In person