The DIAMOND collection is designed for all members of clinical and translational research teams. It includes a variety of items in a range of learning levels regardless of cost. Items can be submitted to the collection through the submission form. There are a limited number of required fields, as well as additional fields that are optional. You can find more information about the Training Materials collection in the FAQ section.

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Trainings from 2019

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Biostatistics Core Seminar Series: "Experimental Study Design", Advance-CTR

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Systematic Review, Advance-CTR

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Biostatistics Core Seminar: "Hypothesis Testing", Advance-CTR, Brown University, Advance-CTR

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Biostatistics Core Seminar Series: "Exploratory Data Analysis", Advance-CTR, Advance-CTR

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Biostatistics Core Seminar Series: "Introduction to Probability", Advance-CTR, Advance-CTR

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Biostatistics Core Seminar Series: "Overview of Study Design", Advance-CTR, Advance-CTR

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Longitudinal Study Design & Ecological and Cross-Sectional Studies, Advance-CTR

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IND and IDE Sponsor and Investigator Training, Duke University

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Essentials of Clinical and Translational Science (ECaTS), Mayo Clinic

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Freely Available Regulatory Science Boot Camp Lectures, Eunjoo Pacifici, Nancy Pire-Smerkanich, and Amelia Spinrad

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Advanced Site Management: Finance and Productivity Enhanced Business Practices for Clinical Research Programs, The Society of Clinical Research Associates

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Clinical Investigator GCP & Trials Management Program for Clinical Investigators and Key Research Staff, The Society of Clinical Research Associates

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Clinical Research Monitoring and GCP Workshop for Monitors, Site Coordinators and Auditors, The Society of Clinical Research Associates

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Clinical Site Coordinator / Manager and GCP Workshop, The Society of Clinical Research Associates

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Emergency Clinical Research Symposium, The Society of Clinical Research Associates

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FDA Clinical Trial Requirements Regulations, Compliance and GCP Conference, The Society of Clinical Research Associates

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'Hot Topics' and Practical Considerations for Protecting Human Research Participants, The Society of Clinical Research Associates

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Oncology Clinical Trials Conference, The Society of Clinical Research Associates

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Pediatric Clinical Trials Conference, The Society of Clinical Research Associates

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Quality Improvement through Standard Operating Procedures (SOPs), The Society of Clinical Research Associates

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PI Responsibilities, The University Of Michigan

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Research Basics: Fundamentals of Data Management, The University Of Michigan

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Clinical Trial Monitoring Module, University of Southern California

Trainings from 2018

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Investigational Drugs and Devices (IND / IDE) Assistance, Harvey Arbit Pharm D, MBA, RAC, CCRP and The Society of Clinical Research Associates (SOCRA)

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What You Should Know Before the FDA Arrives, Harvey Arbit, Pharm D, MBA, RAC, CCRP and The Society of Clinical Research Associates

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Budget Development and Negotiation Training, Duke University

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Study Documentation: Regulations and Best Practices, Duke University

Clinical Research Orientation, Mayo Clinic

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Fundamentals of Clinical and Translational Science (FunCaTS), Mayo Clinic

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Bedside Nursing, JoAnn Mick PhD and The Society of Clinical Research Associates (SOCRA)

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Bedside Nursing - The Journey from Point A to Point B: How to get from Clinical Inquiry to Conducting Nursing Research, JoAnn Mick PhD and The Society of Clinical Research Associates (SOCRA)

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Addicted to Love: Babies born with opiod addiction, Nationwide Children's Hospital

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Bluffing Cancer: Story of drug discovery, Nationwide Children's Hospital

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Can design help medicines fail faster?, Nationwide Children's Hospital

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Health disparaties and mentoring, Nationwide Children's Hospital

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Pediatric diseases: Duchane Muscular Dystrophy and AML, Nationwide Children's Hospital

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Recognizing Unconscious Bias, Nationwide Children's Hospital

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What would happen if we change the way we talk about our research?, Nationwide Children's Hospital

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EQuaTR, Northwestern University

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Mentor Development Workshops, Northwestern University

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Team Science (COALESCE), Bonnie Spring, Holly Falk-Krzesinski, Arlen Moller, Angela Pfammatter, Katya Klyachko, Phillip Rak, and Northwestern University

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A Review of University Policy and Procedures Concerning Scientific Misconduct, The Ohio State University

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But I'm not Exporting Anything: Issues Spotting Export Issues, The Ohio State University

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Clinical Trials and Patient Compensation, The Ohio State University

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COM CR Orientation: Foundations of Clinical Research, The Ohio State University

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Conducting Research with Biorepositories, The Ohio State University

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Considerations for investigational product (IP) transport, The Ohio State University

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Do You Have an SOP for That?, The Ohio State University

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Exempt research, The Ohio State University

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Financial Conflict of Interest in Research: Promoting Integrity, Transparency and Trust, The Ohio State University

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IATA (Dangerous Goods) Training, The Ohio State University

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Informed Consent in Human Subjects Research, The Ohio State University

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Introduction to Human Subjects Research, The Ohio State University

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Investigational Device Exemption (IDE) Sponsor-Investigator Studies, The Ohio State University

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Leadership and Management Styles, The Ohio State University

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Managing Communication and Conflict, The Ohio State University

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OSU Clinical Research Onboarding, The Ohio State University

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Precision Medicine, The Ohio State University

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Predatory Publishing, The Ohio State University

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Project Management in Clinical Research, The Ohio State University

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Rare Disease Research, The Ohio State University

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Research Resources: education and training resources for clinical research coordinators and staff, The Ohio State University

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Research Risks in Human Subjects Research, The Ohio State University

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Canadian Regulatory Conference, The Society of Clinical Research Associates

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Clinical Research / Clinical Science Course, The Society of Clinical Research Associates

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Device Research & Regulatory Conference: The Premier Conference for Device Professionals, The Society of Clinical Research Associates

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cGMP for Investigational New Drugs (IND) in Phase 1 Clinical Trials, The Society of Clinical Research Associates and Harvey Arbit, Pharm D, MBA, RAC, CCRP

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ICH GCP E6 (R2): From the site’s perspective, The Society of Clinical Research Associates and James Simmer BSN, MBA

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Risk-Based Monitoring Clinical Trials, The Society of Clinical Research Associates and James Simmer BSN, MBA

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Best Practices for Social and Behavioral Research, The University Of Michigan

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Budgeting for Research Grants, The University Of Michigan

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Clinical Research Training Workshop, The University Of Michigan

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IMPACT: ClinicalTrials.gov, The University Of Michigan

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IMPACT: Monitoring for Clinical Trials, The University Of Michigan

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IMPACT: Procedure Documentation for Clinical Trials, The University Of Michigan

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MICHR K Writing Workshop, The University of Michigan

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Mock Study Section, The University of Michigan

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Practice Oriented Research Training (PORT), The University of Michigan

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Research Ethics Training for Community Partners, The University Of Michigan

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Responsible Conduct of Research for K Awardees, The University Of Michigan

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Office for Human Subjects Protection Core Training -Module 2 PI Oversight, The University of Rochester

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Office for Human Subjects Protection Core Training - Module 5 Recruitment and Retention, The University of Rochester

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Office for Human Subjects Protection Core Training - Module 7 Investigational Products, The University of Rochester

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Office for Human Subjects Protection Core Training - Module 8 Subject Safety, The University of Rochester

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Office for Human Subjects Protection Core Training - Module 9 Essential Documentation, The University of Rochester

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An Essential Ingredient in Comparative Effectiveness Research, Tufts CTSI

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An Introduction to Mixed Methods, Tufts CTSI

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An Overview of Survey Design, Tufts CTSI

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Applying Mixed Methods Effectively, Tufts CTSI

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Best Practices in Clinical Trials, Tufts CTSI

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Bias and Confounding in Clinical Research, Tufts CTSI

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Calculating Sample Size and Power, Tufts CTSI

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Challenges in Consenting Pregnant Women, Children and Neonates, Tufts CTSI

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Clinical Effectiveness Trials and Predictive Instruments as Decision Support for Implementing CER, Tufts CTSI

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Community Engagement and Input into Comparative Effectiveness Research (CER), Tufts CTSI

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Comparative Effectiveness Research: Recent History and Role in Healthcare Reform, Tufts CTSI

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Comparative Effectiveness Trials, Tufts CTSI

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Concepts of Hypothesis Testing, Tufts CTSI

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Decision Analysis, Tufts CTSI

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Designing a Mixed Methods Study, Tufts CTSI