Research Assistant - 249584 Job at Medix™, Saint Louis, MO

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  • Medix™
  • Saint Louis, MO

Job Description

**SEEKING A CLINICAL RESEARCH ASSISTANT IN ST. LOUIS, MO**

Compensation: $40,000- $52,000

Schedule: Onsite, full time, 40 hrs a week

Location: St. Louis, MO 63128

Job Description:

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 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

Qualifications:

Minimum Qualifications:

• Education:

o High School diploma or the equivalent, with significant relevant experience

o College degree preferred

o Ophthalmic experience preferred

• Experience / Knowledge / Skills:

o Effective oral and written communication

o Delivers safe and appropriate care to patients in addition to the requirements outlined by

study protocols

Job Tags

Full time,

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