Training Requirements
Changes to the type of research activities being conducted or changes to research personnel’s roles and responsibilities may require updates or additional training. It is the responsibility of the principal investigator to ensure all research personnel are adequately trained prior to engaging in research activities.
NEW Clinical Research Coordinator Training Modules
The Office of Research Services (ORS) and ConduITS Institute for Translational Sciences at the Icahn School of Medicine at Mount Sinai have recently added two new CITI Program Learning Modules for clinical research coordinators (or anyone at Mount Sinai) to access educational opportunities.
Mandatory Training for All Research
- CITI Program Training - Financial Conflict of Interest in Research (FCOIR)
- InfoEd Proposal Development Demo 1 (Required for individuals preparing the InfoEd application)
- CITI Research Security Training (Combined) (Required for covered individuals of sponsored project agencies covered under the CHIPS & Science Act and senior/key personnel of NIH sponsored projects submitting other support)
Human Subject Research
Mandatory Training for Human Subject Research
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CITI Program Training
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Human Subjects Research (Basic)
- Investigators/Research Staff Refresher Course
- Data Security and HIPAA Training
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HIPAA Update
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Rigor, Reproducibility, and Ethical Behavior in Biomedical Research
- Good Clinical Practice (GCP)
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Supplemental, Activity Specific Training
- Clinical Research Billing Rules for Investigators
- Epic
- CITI Program Training – OSHA Bloodborne Pathogens
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Radiation Safety Training
To learn which HSR training is required for you click > HERE
Basic Science & Translational Research
- CITI Program Training – Core Training Requirements
- CITI Program Training – Biomedical Research
- Laboratory Specific Safety Orientation
- Certificate of Fitness: C-14
Laboratory Safety Specific Resources
- Laboratory Specific Safety Orientation
- Laboratory Specific Hazard Assessment
- Laboratory Specific Standard Operating Procedures (SOPs)
Supplemental, Activity Specific Training
- CITI Program Training – OSHA Bloodborne Pathogens
- CITI Program Training – Animal Users
- CITI Program Training – Recombinant DNA & Synthetic Nucleic Acids
CITI Program Training – Nanotechnology - CITI Program Training – Shipping Regulated Biological Materials
- CITI Program Training – Dual Use Research of Concern (DURC)
- CITI Program Training – ISMMS Select Agents and Toxins Program
- CITI Program Training – BSL-3/ABSL-3 Biocontainment Research
- CITI Program Training – Autoclave Safety
- CITI Program Training – Biological Safety Cabinets (BSCs)
- Compliant Operation and Management of Dark Rooms (PEAK)
- Eyewashes and Safety Showers (PEAK)
- Initial and Refresher Laser Safety for Researchers (PEAK)
- Initial and Refresher Radiation Safety for Researchers (PEAK)
- Proper Use of Chemical Fume Hoods (PEAK)
Mandatory Training for In Vivo Research
- Institutional Animal Care and Use Committee (IACUC) Training
- CITI Program Training
- Annual Occupational Health and Safety Questionnaire (OHSQ)
Grants Training
- GCO 101: Basics of the Sponsored Project and Research Application Process
- GCO 102: Finding Funding Opportunities Using SPIN
- GCO 201: Basics of Sponsored Projects Budgeting
- GCO 202: NIH Modular Grant Budgets
- GCO 203: Budgeting Direct Costs on Federal Awards
- GCO 204: Budgeting Indirect Costs on Federal Awards
- GCO 301: Preparing Grants with Subawards
- GCO 401: Preparing an NIH Other Support Page
- GCO 402: Collecting Information for the NIH Other Support (OS) Page
- GCO 403: Other Support Template Training
InfoEd Training
Learn how to use InfoEd, the software program, Mount Sinai uses to internally route and manage all research and sponsored project applications. Mount Sinai also uses InfoEd to submit single project, competitive Federal applications. These classes are offered in PEAK on line on demand.
Access
Go to PEAK > OnLine Courses > Functional > Research
Classes
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InfoEd Proposal Development Demo 1
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Creating a new record
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Required Course: Persons preparing the application in InfoEd are required to take this class.
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InfoEd Proposal Development Demo 2
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Creating a Non Competitive Continuation
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InfoEd Proposal Development Demo 3
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Creating a Budget
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InfoEd Proposal Development Demo 4
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Creating a Single Project, Competitive Federal Application (S2S)
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Specialized Training and Permits
- IATA-Dangerous Goods Transport Training
IRB University
The PPHS IRB University Program offers training courses for investigators and research teams who are involved in the design, conduct, and/or reporting of human subject studies at the Mount Sinai Health System. The courses provide hands-on training on the IRB submission requirements, protocol, and consent writing, as well as useful tips to ensure documentation is complete and compliant.
- IRB 101: Basic Steps of the IRB Submission
- IRB 201: Document Analysis & Evaluation: Protocol and Consent
- IRB 300: Series for Request to Rely (R2R) Submissions
- IRB 400: Series for Request to Serve (R2S) Submissions
Training is available in PEAK.
OnCore Training
In order to obtain a User Account within the OnCore Clinical Trials Management System, specific training courses must be submitted in an OnCore/Payments Service Desk User Request. The specific training is dependent upon the user’s role within the system, and is accessed through self-assigned eLearning modules in PEAK.
Find specific Instructions for Access and Training here on the Research Roadmap or by visiting the (Non-Cancer) OnCore Training SharePoint Site.
Contact the OnCore Central team for more information.
Research 411 Portal
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