Introduction

Nurses, are you tired of bedside nursing? Foreign MDs, are you tired of waiting for Residency? 4 Weeks of Training in CDI or CRA or both will change your life

CDI salary: $91k -140k start!!
CRA salary: $95k-165k start!!

4-Week Comprehensive Training

Tuition: $2,000 for CDI or CRA | $3,000 for Both (Bundle & Save $1,000!)

Schedule: 2 hours per day (Evenings) | 4 days per week

Fast-track your career in just one month.

The Instructor has an MD degree, CDIP Certified, >10yrs CRA, Pharmacovigilance and Clinical Scientist Experience, >5yrs CDI experience, >5yrs EMR experience, etc.

4.9 (100+ review)

CLINICAL DOCUMENTATION INTEGRITY (CDI)

Preparation for CDIP & CCDS Exams 

Who Can take this class: MD (US & IMGs), NP, PA, RN, LVN/LPN.

4-Week CDI Training Curriculum

Week 1: The Foundation of CDI & Reimbursement

  • Introduction to CDI: The role of the CDI specialist, professional ethics, and the impact on patient care and hospital revenue.
  • The IPPS System: How hospitals are paid (Inpatient Prospective Payment System) and the basics of MS-DRGs (Medicare Severity Diagnosis Related Groups).
  • Coding Basics for Clinicians: Introduction to ICD-10-CM and PCS; understanding “Clinical Language”
  • Case Studies: Reviewing simple patient charts to identify the Principal Diagnosis (PDX).

Week 2: Advanced Clinical Indicators & Severity

  • Complications & Comorbidities: Mastering CCs and MCCs (Major Comorbidities) to reflect patient complexity.
  • Sepsis & Infectious Disease: Clinical vs. coding definitions of Sepsis 2 and Sepsis 3, and the documentation needed for causative organisms.
  • Respiratory & Cardiac Focus: Documenting Acute Respiratory Failure, Pneumonia types, and CHF acuity (Systolic vs. Diastolic).
  • SOI & ROM: Understanding Severity of Illness and Risk of Mortality metrics.

Week 3: The Query Process & Compliance

  • The Art of the Query: How to write compliant, non-leading queries to physicians (written vs. verbal).
  • Effective Communication: Strategies for MD/PA/NP engagement and overcoming “query fatigue.”
  • HACs and PSIs: Identifying Hospital-Acquired Conditions and Patient Safety Indicators to prevent quality-score penalties.
  • Present on Admission (POA): The importance of documenting conditions found in the ER versus those developed during the stay.

Week 4: Real-World Application & Career Launch

  • Full Chart Reviews: End-to-end review of complex surgical and medical records using electronic health record (EHR) simulators.
  • Denial Prevention: Documenting to defend against RAC (Recovery Audit Contractor) audits and insurance denials.
  • CDI Metrics: Understanding your own performance through “CC/MCC Capture Rates” and “Query Response Rates.”
  • Career Transition: Resume tailoring for CDI, interview prep for non-clinical roles, and networking in the CDI community.

Class Logistics Summary

  • Schedule: 2 hours per day, 4 days per week.
  • Structure: 45 mins Lecture / 45 mins Interactive Chart Review / 30 mins Live Query Workshop.
  • Outcome: Readiness for entry-level CDI roles or preparation for the CCDS/CDIP apprentice exams.
Students Trained
0 +
Interviewing
0 +
Currently Working
0 +
CLINICAL RESEARCH ASSOCIATE (CRA)

Who Can take this class:  Clinical & Non-clinical background, as long as you can perform these 6 skills: Communication, Relationship management, Attention to detail, Critical thinking, Time management, Stress management.

4-Week CRA Training Curriculum

Program Goal

Prepare trainees to function as entry-level or bridge-level CRAs with:

Monitoring readiness (on-site & remote)

  • Strong GCP/regulatory knowledge
  • Source Data Verification (SDV) skills
  • Industry documentation mastery

Week 1: Regulatory Foundations & Study Start-up

  • Overview of Clinical Trials (Phase I–IV)
  • Roles & Responsibilities:
    • Sponsor
    • CRO
    • Principal Investigator (PI)
    • CRA vs CRC
  • Introduction to FDA regulations
  • ICH-GCP Guidelines (E6 R2)

Key Concepts

  • Informed Consent Process (ICP)
  • Protocol structure & interpretation
  • Adverse Events (AE) vs Serious Adverse Events (SAE)

WEEK 2: REGULATORY & DOCUMENTATION MASTERY

Topics Covered

  • Essential Documents (Trial Master File – TMF)
  • Investigator Site File (ISF)
  • Regulatory Submissions (IND, NDA basics)
  • Institutional Review Board (IRB) process

 Key Concepts

  • ALCOA-C principles (data integrity)
  • Protocol deviations vs violations
  • Audit readiness

Topics Covered

  • Monitoring Visit Types:
    • Site Initiation Visit (SIV)
    • Routine Monitoring Visit (RMV)
    • Close-Out Visit (COV)
  • Source Data Verification (SDV)
  • Case Report Forms (CRFs) & eCRFs
  • Query management

Key Concepts

  • Risk-Based Monitoring (RBM)
  • Data discrepancies & resolution
  • Protocol compliance

4: ADVANCED CRA SKILLS + JOB READINESS

Topics Covered

  • Remote Monitoring & EDC systems (Medidata, Oracle, Veeva)
  • Safety reporting workflows
  • Site management & communication
  • Sponsor/CRO expectations

Key Concepts

  • Inspection readiness (FDA audits)
  • CAPA (Corrective and Preventive Actions)
  • Risk mitigation strategies

Resume & Interview Prep

  • CRA resume building (CRO-focused)

REGISTERATION

Are you ready to make that change?

Easy Process, just follow the instructions below. Enter your name, email, phone# and make a selection of your interest

Subscription Form
No payment items has been selected yet

CONTACT US

Are you ready?

Classes are  4 days / week, 2 days to teach CDI and 2 days for CRA.

© 2026 LearnMedJobs. All rights reserved.