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Entry Level International Medical Chart Review Jobs

University of Virginia

Medical Scribe

Charlottesville, VA · On-site

$15 - $21.16/hr

Performs random chart reviews for quality assurance medical documentation purposes. * Keeps chart deficiencies to less than 5%. * Assists the physician with communicating their patient care plans ...

OneLegacy

Ocular Recovery Technician

Azusa, CA · On-site

$18 - $22.75/hr

The ORT performs medical chart review, plasma dilution review, medical screening criteria review, and qualifies donor for recovery eligibility. The ORT also performs housekeeping and the facility ...

OneLegacy

Ocular Recovery Technician

Azusa, CA · On-site

$47K - $62K/yr

The ORT performs medical chart review, plasma dilution review, medical screening criteria review, and qualifies donor for recovery eligibility. The ORT also performs housekeeping and the facility ...

Community Care Physicians (CCP)

Certified Coder

Latham, NY · On-site +1

$22 - $29.25/hr

Strong knowledge of medical terminology, anatomy and physiology, and medical chart review required. * Knowledge of ICD-10 diagnosis and procedure codes, CPT codes, and HCPCS codes required.

Community Care Physicians

Certified Coder

Latham, NY · On-site

$22.40 - $33.60/hr

Strong knowledge of medical terminology, anatomy and physiology, and medical chart review required. * Knowledge of ICD-10 diagnosis and procedure codes, CPT codes, and HCPCS codes required.

Adventist Health

Chart Auditor - Glendale

Glendale, CA · On-site

Current licensed RN in the state of practice (RN), medical provider (MD), or International Medical ... Reviews medical records to validate patient placement (inpatient vs. observation) against payer ...

Adventist Health

Chart Auditor (Portland)

Portland, OR · On-site

$52.55 - $78.77/hr

Current licensed RN in the state of practice (RN), medical provider (MD), or International Medical ... Reviews medical records to validate patient placement (inpatient vs. observation) against payer ...

Adventist Health

Chart Auditor - Glendale

Glendale, CA · On-site

$62.83 - $86.18/hr

Current licensed RN in the state of practice (RN), medical provider (MD), or International Medical ... Reviews medical records to validate patient placement (inpatient vs. observation) against payer ...

Adventist Health

Chart Auditor (Portland)

Portland, OR · On-site

Current licensed RN in the state of practice (RN), medical provider (MD), or International Medical ... Reviews medical records to validate patient placement (inpatient vs. observation) against payer ...

Methodisthealthsystem

CLIN DOCUMENTATION SPEC I

Dallas, TX

$34.50 - $46.25/hr

Perform thorough initial and concurrent medical chart reviews identifying opportunities for documentation improvement. Verify that all treated or monitored conditions are properly documented by the ...

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International Medical Graduate (IMG) - Clinical Research Coordinator

Revival Research Institute, LLC

Elgin, IL • On-site

$24 - $32/hr

Full-time

Re-posted 2 days ago

Job description

Unique opportunity to make an Impact in the healthcare industry...
Revival Research Institute, LLC was established in 2015, and headquartered in the Metro Detroit Region, and has been growing ever since. Revival now has a national presence in the Metro-Detroit Region, Texas, Illinois, and Arizona. We have been nationally acknowledged for our diligence to provide the highest quality of data for our clinical research trials.
As Revival Research Institute is growing, we are looking to add more qualified professionals to our team, who are looking for an opportunity to grow and learn with us.
We are seeking International Medical Graduates with a minimum of 3 year of research experience and Psych back ground. Additionally, someone with a strong interest in the Clinical Research field would be an excellent fit for our entry level position, with room to grow. However, this interest and background is not necessary, as our ideal candidate is an individual who is detail orientated, being able to maintain organized records, as well as someone who is motivated to learn new things, as our company is always growing and expanding into new therapeutic areas. We are looking for individuals that want the opportunity to learn and grow with us.
New Staff should be genuinely respectful of diverse points-of-view and strive for an environment in which inclusiveness drives productivity and results. Some responsibilities will include coordinating and managing multiple studies. They are also responsible for assisting the Principal Investigators and other clinical staff, with any study related tasks as follows but not limited to:
  1. Research participant screening, recruitment and enrollment. Consent and conduct research visits for data collection/no risk trials or no study article/minimal risk trials with oversight. Responsible for collecting, processing and shipping of research specimens, where applicable.
  2. Document study related information in case report forms or electronic data capture systems, handles data queries and participates in monitoring visits. Obtain, review and maintain source documents.
  3. Maintain organization of all trial related documents and correspondence. Implement quality control and assurance methods.
  4. Communicate with study sponsors, research team and the Institutional Review Board. Assist with basic regulatory document preparation, with oversight e.g. study amendments, adverse event reporting, protocol deviation reporting.
  5. Maintain professional and technical knowledge of Clinical trials and Standards of Care.
  6. Protect patient confidentiality.

Preferred Qualifications
  1. Education/ Training: International Medical Graduate; MBBS, BMBS, MBChC, MBBCh, MD, DO, MCM, DM, MCM, MMSc, MMedSc, MM, MMed, MS, MSurg, MChir, MCh, ChM, CM, MSc, DCM, DClinSurg, DMSc, DMedSc, DS, DSurg
  2. Radiology experience is preferred. Phlebotomy skills are also preferred.
  3. Additional Qualifications: Database and computer skills: Microsoft Office (Word, Excel), Outlook, excellent verbal and written communication skills, ability to work independently and assume responsibility, excellent organizational skills, ability to meet data deadlines and maintain confidentiality. Maintain data integrity within the department. Must be able to work in a team consisting of physicians, nurses, technicians, secretarial staff and ancillary hospital staff. Knowledge of FDA Regulations and Good Clinical Practices.

JOIN US & GROW YOUR KNOWLEDGE & EXPERIENCE!!!

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