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It covers staff readiness tasks such as facility orientation, access provisioning, contact list distribution, and administrative documentation, followed by mandatory trainings across safety, privacy, biosafety, harassment prevention, and emergency preparedness. 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Use Non-applicable (N/A) if needed. |\n| --- | --- | --- |\n| Employee Badge | 1-week before\u003Cbr>start | AK |\n| Parking | 1-week before\u003Cbr>start | N/A |\n| Benefits enrollment | 1-week before\u003Cbr>start | AK |\n| Orientation (HR, employee health, IT) | Day one | AK |\n| Staff Respectful Workplace | Day one | AK |\n| Tour of Facilities | Day one | N/A |\n| Meet with team members | Day one | AK |\n| The review process for clocking in/out and submitting Paid Time Off (PTO) requests | Day one | AK |\n| Receive departmental contact lists | Day one | AK |\n| W4 and Direct deposit forms | Day one | AK |\n| Staff Handbook acknowledgment | Day one | AK |\n| Door Access/Codes | Day one | AK |\n| Added staff to all mandatory meeting invitations | First week | N/A |\n| Added to share drives, Microsoft Teams, Intranet Access | First Week | N/A |\n| Review of frequently used websites and resources | First Week | N/A |\n| Telephone/Voicemail setup | First week | N/A |\n| Standard Operating Procedures | 1-2 weeks | AK |\n| Corrective/preventative Action Plans | First month | AK |\n\n\n| Mandatory Training | Suggested Timeline | Provide requirements for observations (OBS), acknowledgment (AK), or return demonstrations (RD. Use Non-applicable (N/A) if needed. |\n| --- | --- | --- |\n| COVID-19 Hygiene Best Practices | 1-2 weeks |  |\n| Bloodborne Pathogens Training | 1-2 weeks | AK |\n| Fire/Life Safety | 1-2 weeks |  |\n| How to report information to regulatory authorities | 1-2 weeks |  |\n| HIPAA/Protecting Patient Privacy | 1-2 weeks |  |\n| Biosafety standards | 1-2 weeks |  |\n| Harassment Prevention for nonSupervisors | 1-2 weeks |  |\n| Chemical Safety | 1-2 weeks |  |\n| Hazardous Communications | 1-2 weeks |  |\n| Hazardous Drugs Spill Clean Up | 1-2 weeks |  |\n| Safety Documentation and Reporting | 1-2 weeks |  |\n| Diversity and Inclusion | 1-2 weeks |  |\n| Emergency preparedness | 1-2 weeks |  |\n| HIPAA Privacy for Researchers | 1-month |  |\n\n\n| Basic medical terminology\u003Cbr>training/Common research terminology | 1-month |  |\n| --- | --- | --- |\n| Acronym List | 1-month |  |\n| State and Country Specific Regulations | 1-month |  |\n| Shipping Biological Materials | 1-month |  |\n| Good Documentation Practices | 1-month |  |\n| Adverse Events: Identify, Document, Report | 1-month |  |\n| Introduction to Informed Consent | 1-month |  |\n| The Informed Consent Process | 1-month |  |\n| Informed Consent, remote or eConsent | 1-month |  |\n| Health System Violence Awareness Training and Armed and Dangerous Training | 1-month |  |\n| Food and Drug Administration (FDA) Regulations and Guidance | 1-month |  |\n| How to Read a Research Protocol | 1-month |  |\n| Unconscious Bias\u003Cbr>Training | 1-month |  |\n| Shipping Training | 1-3 months |  |\n| Study Financial Management | 1-3 months |  |\n| Research Budgeting | 1-3 months |  |\n| Coverage Analysis | 1-3 months |  |\n| IRB eProtocol Training | 1-3 months |  |\n| General and Institutional Review Board (IRB) Reporting Requirements | 1-3 months |  |\n| Ethics and Clinical Research | 1-3 months |  |\n| Cancer Education 101 | 1-3 months |  |\n| Cheson/Lugano, IMWG, iwCLL, RANO etc. as applicable |  |  |\n| RECIST Response Evaluation Criteria in Solid Tumors (RECIST) | 1-3 months |  |\n| Clinical Research 101 | 1-3 months |  |\n| The Revised Common Rule for Human Subjects’ Protections | 1-3 months |  |\n| Responsible Research Conduct | 1-3 months |  |\n| General Research Safety Training | 1-3 months |  |\n| Privacy for Research | 1-3 months |  |\n| Conflict of Interest (COI) | 1-3 months |  |\n| Environment of Care (Setting of Care) | 1-3 months |  |\n| Infection Control for Non-clinical Staff | 1-3 months |  |\n| Time-out Training Module | 1-3 months |  |\n| Tuberculosis (TB) Training | 1-3 months |  |\n| 21st Century Cures Act | 1-3 months |  |\n|","cbCaiqt04Ake6NJP","https://ap.wps.com/l/cbCaiqt04Ake6NJP","pdf",184610,6,"English","# Onboarding\n# Mandatory Training\n# Basic medical terminology and research terminology\n# Cancer and clinical research trainings\n# Computer systems trainings","[{\"question\":\"What does the checklist require for onboarding activities?\",\"answer\":\"It lists onboarding steps with a suggested timeline and specifies evidence requirements such as observation (OBS), acknowledgement (AK), or return demonstrations (RD).\"},{\"question\":\"Which mandatory training topics are included?\",\"answer\":\"Mandatory topics include COVID-19 hygiene best practices, bloodborne pathogens, fire/life safety, regulatory reporting, HIPAA privacy protection, biosafety standards, harassment prevention, chemical safety, and emergency preparedness.\"},{\"question\":\"How are research-related trainings organized in the template?\",\"answer\":\"Research trainings are grouped into modules such as medical and common research terminology, informed consent process and remote/eConsent, research protocol reading, documentation and adverse event reporting, and regulatory or ethical conduct topics.\"},{\"question\":\"What format is used to indicate evidence and timing for trainings?\",\"answer\":\"The template uses a table with a suggested timeline and a column that indicates observation (OBS), acknowledgement (AK), or return demonstrations (RD), using N/A where applicable.\"}]","Standard Training Checklist Template - Onboarding - Mandatory Training - Basic Medical Terminology | PDF",1790378369]