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  • Skills you'll gain: Drug Interaction, Pharmacology, Pharmaceuticals, Pre-Clinical Development, Drug Development, Pharmacotherapy, Biochemical Assays, Laboratory Testing, Medication Administration, Pharmaceutical Terminology, Clinical Research, Laboratory Research

  • Skills you'll gain: Good Clinical Practices (GCP), Informed Consent, Institutional Review Board (IRB), Clinical Research Ethics, Clinical Research Coordination, Clinical Research, Clinical Trials, Clinical Data Management, Drug Development, Record Keeping, Clinical Documentation, Regulatory Compliance, Document Management, Health Equity, Patient Communication

  • Johns Hopkins University

    Skills you'll gain: Clinical Data Management, Clinical Trials, Clinical Monitoring, Sample Size Determination, Clinical Research Ethics, Clinical Research, Data Quality, Healthcare Ethics, Quality Assurance, Clinical Trial Management Systems, Good Clinical Practices (GCP), Case Report Forms, Institutional Review Board (IRB), Data Maintenance, Data Cleansing, Data Management, Regulatory Compliance, Data Integrity, Informed Consent, Data Collection

  • Skills you'll gain: Clinical Data Management, Data Quality, Quality Assurance, Clinical Trial Management Systems, Case Report Forms, Clinical Trials, Data Maintenance, Clinical Monitoring, Data Cleansing, Data Management, Data Integrity, Clinical Research, Microsoft Excel, Data Compilation, Data Collection, Data Sharing, Data Security, Treatment Planning, Statistical Analysis

  • Skills you'll gain: Team Motivation, Team Management, Clinical Leadership, Patient Communication, Team Performance Management, Team Leadership, Constructive Feedback, Team Building, Emotional Intelligence, Healthcare Project Management, Decision Making, Communication Strategies, Conflict Management, Project Management, Leadership and Management, Leadership, Communication, Empathy, Empathy & Emotional Intelligence, Health Care

  • Skills you'll gain: Health Disparities, Health Equity, Diversity Training, Clinical Trials, Clinical Research, Diversity Awareness, Clinical Research Ethics, Diversity Equity and Inclusion Initiatives, Cultural Diversity, Cultural Sensitivity, Mitigation, Health Care, Healthcare Ethics

What brings you to Coursera today?

  • Skills you'll gain: Analytics, Predictive Analytics, Applied Machine Learning, Predictive Modeling, Science and Research, Machine Learning, Clinical Data Management, Medical Science and Research, Biomedical Technology, AI Integrations, Generative AI, AI literacy, Regulatory Compliance

  • Skills you'll gain: Patient Registration, Medical Records, Medical Billing and Coding, Medical Office Procedures, Health Insurance Portability And Accountability Act (HIPAA) Compliance, Patient Communication, Health Information Management, Revenue Cycle Management, Electronic Medical Record, Records Management, Clinical Documentation, Patient Safety, Care Coordination, Data Entry, Scheduling, Inventory Management System, Medical Terminology, Regulatory Compliance, Key Performance Indicators (KPIs), Quality Assurance

  • Status: Job Ready

    Johns Hopkins University

    Skills you'll gain: Medical Billing and Coding, Denial Management, Patient Registration, Care Management, Medical Privacy, Revenue Cycle Management, Practice Management, Organizational Change, Change Management, Health Insurance Portability And Accountability Act (HIPAA) Compliance, Performance Review, Data Management, ICD Coding (ICD-9/ICD-10), Medical Terminology, Claims Processing, Medical Billing, Patient Safety, Continuous Quality Improvement (CQI), Medical Management, Data Analysis

  • Skills you'll gain: Clinical Data Management, Data Capture, Electronic Data Capture (EDC), Clinical Research, Data Management, Data Collection, Data Sharing, Data Entry, Data Strategy, Data Quality, Data Storage, Regulatory Compliance

  • Skills you'll gain: Good Clinical Practices (GCP), Clinical Research, Clinical Trials, Clinical Research Ethics, Informed Consent, Clinical Data Management, Drug Development, Health Equity

  • Skills you'll gain: Good Clinical Practices (GCP), Informed Consent, Clinical Research Coordination, Clinical Research, Clinical Trials, Clinical Research Ethics, Institutional Review Board (IRB), Drug Development, Record Keeping, Clinical Documentation, Regulatory Compliance, Patient Communication