
Microsoft
Skills you'll gain: Stakeholder Engagement, Stakeholder Analysis, Stakeholder Management, Stakeholder Communications, Data Ethics, Compliance Management, Leadership Studies, Business Ethics, Governance, Governance Risk Management and Compliance, Regulatory Compliance, Business Leadership, Compliance Reporting, Change Management, Ethical Standards And Conduct, Accountability Frameworks, Leadership and Management, Risk Management, Microsoft Teams, Microsoft Visio
Advanced · Course · 1 - 3 Months

Sage Publications
Skills you'll gain: Institutional Review Board (IRB), Research Design, Informed Consent, Research, Ethical Standards And Conduct, Law, Regulation, and Compliance
Intermediate · Course · 1 - 3 Months

Skills you'll gain: Nursing Management, Healthcare Ethics, Clinical Leadership, Personal Integrity, Nursing, Patient Safety, Ethical Standards And Conduct, Nursing Practices, Health Care Procedure and Regulation, Decision Making, Accountability, Risk Management, Health Care, Medical Privacy, Informed Consent, Regulatory Compliance
Intermediate · Course · 1 - 4 Weeks

Utrecht University
Skills you'll gain: Epidemiology, Clinical Practices, General Medicine, Clinical Research, Medical Science and Research, Diagnostic Tests, Clinical Trials, Public Health, Patient Treatment, Predictive Modeling
★ 4.7 (422) · Intermediate · Course · 1 - 3 Months

Peking University
Skills you'll gain: Nursing, Science and Research, Nurse Education, General Science and Research, Clinical Research, Scientific Methods, Nursing and Patient Care, Clinical Research Ethics, Medical Science and Research
★ 4.8 (6) · Intermediate · Course · 1 - 3 Months

American Psychological Association
Skills you'll gain: Institutional Review Board (IRB), Research, Scientific Methods, Ethical Standards And Conduct, Research Methodologies, Case Studies, Informed Consent, Psychology, Research and Design, Cultural Diversity, Diversity Awareness
★ 4.8 (86) · Beginner · Course · 1 - 3 Months

Johns Hopkins University
Skills you'll gain: Clinical Trials, Clinical Research Ethics, Clinical Research, Healthcare Ethics, Scientific Methods, Statistical Reporting, Ethical Standards And Conduct, Drug Development, Statistical Methods, Statistical Analysis
★ 4.7 (4.4K) · Mixed · Course · 1 - 3 Months

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
★ 4.8 (233) · Beginner · Course · 1 - 4 Weeks

Universidad Nacional Autónoma de México
Skills you'll gain: Institutional Review Board (IRB), Clinical Research Ethics, Medical Science and Research, Healthcare Ethics, Informed Consent, Clinical Research, Scientific Methods, Statistical Methods, Sampling (Statistics), Statistical Analysis, Quantitative Research, Science and Research, Responsible AI, Biostatistics, Technical Writing, Sample Size Determination, Statistical Inference, Statistical Hypothesis Testing
★ 4.9 (97) · Beginner · Course · 3 - 6 Months

Skills you'll gain: Patient-centered Care, Clinical Supervision, Clinical Experience, Healthcare Ethics, Basic Patient Care, Patient Communication, Patient Advocacy, Dignity in Care, Patient Treatment, Patient Safety, Patient Evaluation, Health Care, Ethical Standards And Conduct, Health Assessment, Professionalism, Communication, Healthcare Industry Knowledge, Empathy, Decision Making, Critical Thinking and Problem Solving
Beginner · Course · 1 - 4 Weeks

Genentech
Skills you'll gain: Clinical Data Management, Clinical Trials, Clinical Research, Interactive Data Visualization, Case Report Forms, Drug Development, Data Presentation, R (Software), Pharmaceuticals, Shiny (R Package), Data Visualization, Statistical Reporting, Dashboard, Data Modeling, R Programming, Data Manipulation, Statistical Programming, Data Science, Statistical Analysis, Data Preprocessing
★ 4.6 (19) · Intermediate · Course · 1 - 3 Months

Skills you'll gain: Drug Development, Clinical Trials, Clinical Research, Clinical Research Coordination, Informed Consent, Good Clinical Practices (GCP), Clinical Research Ethics, Pharmacology, Clinical Data Management, Pre-Clinical Development, Pharmaceuticals, Biostatistics, Clinical Monitoring, Institutional Review Board (IRB), Patient Safety, Research, Clinical Documentation, Communication, Technical Writing, Marketing
★ 5 (10) · Mixed · Course · 1 - 3 Months