On Research - With CITI Program podcast

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World of Secrets

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The Killing Call: 1. The death of a star 35:12

7일 전35:12

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35:12

Sidhu Moose Wala explodes onto the Canadian music scene. His sound is a fusion of two worlds - hip-hop with the poetic language of rural Punjab, where he is from. After years of struggle he’s making it. But with the spotlight comes a dark side. As his fame grows, so do the threats. "We will kill you." Presented by broadcaster and DJ Bobby Friction and investigative journalist Ishleen Kaur. Season 8 of World of Secrets, The Killing Call, is a BBC Eye investigation for the BBC World Service. Archive audio credits: Lovepreet Waraich, Malwa TV, BritAsia TV, MPHONE Canteeni Mandeer, GK Digital, Thakur Media, Capital Extra, Famous Punjab TV, ModernSings, Dheeth.jeha, RealRohitBlogs, Mirror Now, India Today. Here’s a link to the BBC Eye two-part documentary films, which we recommend you watch after listening to this podcast: https://bit.ly/thekillingcall If you are in the UK, you can watch on iPlayer: https://www.bbc.co.uk/programmes/m002f18y…

On Research - with CITI Program

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Discussing issues that impact scientific research monthly, from clinical research to ethical considerations. Hosted by Alexa McClellan. New episode every month. Learn more at about.citiprogram.org

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On Research - with CITI Program

updated 22일 전

시리즈 홈•Feed

Discussing issues that impact scientific research monthly, from clinical research to ethical considerations. Hosted by Alexa McClellan. New episode every month. Learn more at about.citiprogram.org

30 에피소드

#Science #CITI Program

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On Research - with CITI Program

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Engaging with Online Communities: Ethical Considerations for Researchers - On Research Podcast 38:08

22일 전38:08

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38:08

How do we responsibly study digital communities without violating their trust? Where do we draw the line between research and interference? Joining us today is Dr. Sarah Gilbert, a research associate at Cornell University and research director of the Citizens and Technology Lab. Her work focuses on supporting healthy online communities, including how online data can be reused ethically. Together, we'll unpack the CMV subreddit case, explore how current research norms are being tested in real time, and ask what a more transparent future might look like. Additional resources: Research papers about ethical research on Reddit: Remember the Human: A Systematic Review of Ethical Considerations in Reddit Research - https://dl.acm.org/doi/abs/10.1145/3633070 Cross-Platform user expectations for social media data reuse - https://journals.sagepub.com/doi/full/10.1177/20539517231164108 Guides: Association for Internet Researchers: Internet Research: Ethical Guidelines 3.0 - https://aoir.org/ethics/ PERVADE Data Ethics Tool - https://pervade.umd.edu/pervade-data-ethics-tool/ AskHistorians Policy for Researchers using r/AskHistorians in Research - https://www.reddit.com/r/AskHistorians/comments/1iu4otk/meta_new_policy_for_researchers_using/ Excavating awareness and power in data science: A manifesto for trustworthy pervasive data research - https://journals.sagepub.com/doi/full/10.1177/20539517211040759 Beyond the Individual: A Community-Engaged Framework for Ethical Online Community Research - https://arxiv.org/pdf/2503.13752 Tool for large-scale disclosure: Procedural and Substantive Ethics in the Design of Research Ethics Systems - https://journals.sagepub.com/doi/10.1177/20563051221077021…

On Research - with CITI Program

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CITI Program Turns 25: A Celebration of Commitment to Research Integrity - On Research Podcast 36:37

7 weeks 전36:37

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36:37

Today’s episode is a celebration of CITI Program’s 25th anniversary. We talk with a panel of long-time employees, including Jaime Arango, Vice President of Content and Education, Daniel Smith, Director of Content and Education, and Adiper Bello, Director of Operations and Support, about the history of CITI Program, key milestones in the company, and where CITI Program is headed. Additional resources: CITI Program timeline: https://about.citiprogram.org/get-to-know-citi-program/…

On Research - with CITI Program

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Community Engagement in Research - On Research Podcast 1:05:38

12 weeks 전1:05:38

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1:05:38

Join us for a fascinating discussion with Dr. Jeremy Rossman, a researcher of 25 years, virologist, and President of a non-profit aimed at creating lasting and sustainable community development in research worldwide. We take a deep dive into community engagement in research; what it means, the challenges and opportunities, and why it’s so important. Jeremy does a wonderful job of explaining community engagement from all sides, whether you’re the researcher, the community involved in the research, or the funding agency; it really takes all parties involved to work collaboratively towards improving research. A special thank you to Cynthia Bellas for helping produce this episode! Guest Bio: Dr. Jeremy Rossman is a virologist, President of the non-profit organization Research-Aid Networks, and an Honorary Senior Lecturer in Virology at the University of Kent. Dr. Rossman has conducted collaborative interdisciplinary research on the molecular biology of pandemic-causing viruses, international epidemic responses, evidence-based humanitarian aid and science education. Research-aid networks facilitate collaborative and evidence-based approaches for assessing need, delivering aid, evaluating effectiveness, and achieving equitable, long-term, sustainable community development worldwide. Additional Resources: Dr. Rossman’s Non-Profit Research-Aid Networks - https://researchaidnetworks.org/ NIH Community Engagement Alliance - https://ceal.nih.gov/ Long-COVID Patient-Led Research Collaborative - https://patientresearchcovid19.com/ Learn more about HRP Consulting here - https://thehrpconsultinggroup.com/ Learn more about CITI Program at about.citiprogram.org .…

On Research - with CITI Program

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Dual Use Research of Concern Policy - On Research Podcast 41:03

16 weeks 전41:03

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41:03

Join us for a fascinating discussion about the recently updated Dual Use Research of Concern policy. There was so much to cover that I brought in two experts – one as my co-host and the other as our guest. If you don’t know much about Dual Use Research of Concern, this conversation will be a fantastic primer. We discuss what Dual Use means, the policy updates, how these updates could impact your research institution, and why all of this matters. Also of note, we recorded this episode a couple of weeks ago, in the midst of the many executive orders impacting research. Anne and Melissa do share their thoughts on how you should move forward in this gray area we’ve all found ourselves in, but we always encourage folks to stay up to date as much as possible on the evolving landscape. Additional Resources: DURC Policy released May 2024, effective May 2025 - https://bidenwhitehouse.archives.gov/wp-content/uploads/2024/05/USG-Policy-for-Oversight-of-DURC-and-PEPP.pdf Implementation Guidance for DURC policy - https://bidenwhitehouse.archives.gov/wp-content/uploads/2024/05/USG-DURC-PEPP-Implementation-Guidance.pdf Learn more about HRP Consulting: https://thehrpconsultinggroup.com/ Learn more about CITI Program at about.citiprogram.org . Guest Bios: Melissa James – Guest – Melissa is the BSL-3 Facility Manager for Yale University with 12+ years of high containment experience, including establishing and maintaining compliance with the Federal Select Agent Program. Her degrees in biology and Homeland Security and RBP credentials position her to share her vast knowledge and experience with others in the field. Anne Hawkinsbadge – Guest Host – Anne is the Assistant Director of EHS. She is a Certified Safety Professional, Certified Healthcare Safety Professional, Certified Healthcare Emergency Professional, and a Chemist with the American Society of Clinical Pathology. Her work experience includes healthcare, auto manufacturing, pharmaceutical, academia, worker compensation insurance, and chemical manufacturing.…

On Research - with CITI Program

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Coverage Analysis in Clinical Research - On Research Podcast 51:04

20 weeks 전51:04

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51:04

Join us for episode 1 of season 3 as we explore an essential compliance topic: coverage analysis. It’s a complicated process, but lucky for us, we have Andra Popa. Andra is an expert with nearly two decades of experience in healthcare law, compliance, and coverage analysis. As one of the first in the industry to provide coverage analysis, Andra walks us through the intricate details of the process, including why it’s so important and the consequences if you don’t have a proper coverage analysis process in place. Additional Resources: Local Coverage Determinations CMS - https://www.cms.gov/medicare/coverage/determination-process/local National Coverage Determinations CMS - https://www.cms.gov/medicare-coverage-database/search-results.aspx?keyword=nat&areaId=all&docType=NCD Thorny Medicare Coverage Issues article by Andra Popa - https://compliancecosmos.org/thorny-medicare-coverage-issues Learn more about HRP Consulting here: https://thehrpconsultinggroup.com/ Learn more about CITI Program at about.citiprogram.org . Guest Bio: Andra Popa is responsible for healthcare content at CITI Programs and was part of the first group to conduct Medicare Coverage Analyses. She owned a consulting firm that worked with over 40 healthcare entities to create, assess, audit, and monitor compliance programs, as well as to create educational programs. A graduate of Boston College with degrees in English and economics, she also has JD and LLM (healthcare law) degrees from Loyola University Chicago School of Law. She has published over 100 articles, written book chapters, and conducted workshops in design and compliance.…

On Research - with CITI Program

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PRIM&R 2024 Conference Recap - On Research Podcast 56:31

27 weeks 전56:31

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56:31

Join us for an engaging recap of the recent PRIM&R conference, held on November 17-20 in Seattle. With an amazing panel of research professionals, we discuss the highlights, popular sessions, hot topics, and the benefits of attending this conference. Whether you attended or not, there is plenty of valuable information shared by the panel of experts in our field. Guest panel for this episode: Jaime Arango, Vice President of Content and Education at CITI Program; Rafaella Hart, Senior Vice President of IRB, IBC & QA at BRANY; Karen Christianson, Senior Vice President and Managing Director of the HRP Consulting Group; Walden Leverich, Senior Vice President and Managing Director of Tech Software; and Nate Ferguson, a consultant and IRB Analyst who collaborates with a variety of clients, including footwear and apparel companies conducting human subjects research. Additional Resources: PRIM&R’s 50th-anniversary blog post - https://blog.primr.org/the-history-of-primrs-conferences/ Learn more about HRP Consulting here - https://thehrpconsultinggroup.com/ Learn more about CITI Program at about.citiprogram.org .…

On Research - with CITI Program

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Updated Research Misconduct Final Rule - On Research Podcast 41:35

27 weeks 전41:35

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41:35

Join us for an in-depth discussion about the updated research misconduct final rule. John Baughman, a research compliance expert, gives an excellent overview of the updates, why they matter, and how to be prepared when the policy goes into effect on January 1, 2025. While we all wait for the templates and guidance documents from the Office of Research Integrity, John provides some excellent advice and breaks down the most important elements of the new final rule. Additional Resources: The Updated Final Rule on Research Misconduct - https://www.federalregister.gov/documents/2024/09/17/2024-20814/public-health-service-policies-on-research-misconduct Blog from ORI about the updated final rule - https://ori.hhs.gov/blog/ori-final-rule Learn more about HRP Consulting - https://thehrpconsultinggroup.com/ Learn more about CITI Program at about.citiprogram.org . Guest Bio: John R. Baumann, Ph.D., was the Associate Vice President for Research Compliance at Indiana University, including the Bloomington and Indianapolis campuses, as well as the five regional campuses and affiliated hospitals. Dr. Baumann has over 25 years of experience in research, research administration, responsible conduct of research, and research compliance. He has had direct-line responsibility for all aspects of research compliance with regulations and ethical standards related to research misconduct, human subjects research, research with animals, conflict of interest, radiation, and biological safety, as well as research development, coordination, and submission of grant and contract applications, and management of funded research.…

On Research - with CITI Program

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The Role of Pharmacy in Research - On Research Podcast 48:17

33 weeks 전48:17

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48:17

Join us for a fascinating discussion about the evolution of pharmacy in clinical research. Adam Samson, Head of Clinical Delivery Operations at Walgreens, discusses how pharmacists and pharmacy techs have more opportunities to participate in clinical trials. Learn how Walgreens has developed its research program to include the pharmacy at the center of its operations. This program includes takeaways that any research organization can learn from, including how best to include pharmacists and techs in future research. Additional Resources: Learn more about clinical trials at Walgreens: https://go.walgreenshealth.com/clinicaltrials Article about the evolving role of pharmacists in research: https://pharmddegree.com/careers/research-pharmacist/ Learn more about HRP Consulting here: https://thehrpconsultinggroup.com/ Learn more about CITI Program at about.citiprogram.org . Guest Bio: Adam Samson has 15 years of experience designing and executing clinical trials across multiple therapeutic areas, phases, and treatment modalities. Adam is a clinical research executive passionate about bringing clinical trials closer to patients through community pharmacies and other innovative models. Adam also serves as an Adjunct Faculty at George Washington University in the Regulatory Affairs and Clinical Research Leadership Graduate Program. He volunteers with several non-profit organizations that aim to improve the clinical research industry through pre-competitive collaborations.…

On Research - with CITI Program

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Practical Uses of AI in Research - On Research Podcast 47:18

38 weeks 전47:18

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47:18

Join us for a deep dive into the world of AI and its practical applications in the world of research operations. Charlie Fremont, an EHR application analyst specializing in research operations and billing, discusses how AI technology has helped him create new workflows that have vastly improved processes. Not only does he share details around how he uses this technology, he also shares valuable insight into the limitations and potential risks of using these tools. We also discuss AI’s impact on productivity in general and sorting through the proper balance of efficiencies with compliance. Additional Resources: The AI Risk Repository: A Comprehensive Meta-Review, Database and Taxonomy of Risks from AI - https://arxiv.org/abs/2408.12622 Deloitte Report – How Generative AI can reshape the health frontier - https://www2.deloitte.com/content/dam/Deloitte/us/Documents/life-sciences-health-care/us-from-code-to-cure-1.pdf Learn more about HRP Consulting: https://thehrpconsultinggroup.com/ Learn more about CITI Program at about.citiprogram.org . Guest Bio: Charlie Fremont is an Epic EHR Application Analyst and independent consultant with extensive research and billing experience. With 15 years in the healthcare industry and 10 years in research, Charlie specializes in leveraging technologies such as ChatGPT, Python, and Excel Formulas/VBA. Charles has successfully implemented solutions that streamline workflows and improve operational efficiency, which he shares openly with colleagues in our research industry.…

On Research - with CITI Program

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Politics and Research: Transferrable Skills - On Research Podcast 43:41

42 weeks 전43:41

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43:41

Join us for a fascinating discussion about the intersection of Research and Politics. Rachel Baker, a research nurse and House Representative in the state of Ohio, discusses working in two very different fields and how they both inform each other. We focus on the similarities of the fields and the transferable skills that Rachel has learned from her political career that have helped in her research role. Additional Resources: Ohio House of Representatives website - https://ohiohouse.gov/members/rachel-b-baker Learn more about HRP Consulting : https://thehrpconsultinggroup.com/ Learn more about CITI Program at about.citiprogram.org . Guest Bio: Rachel Baker has earned a BSN, MSW, and PhD. She works as a Nurse Researcher and teaches Research and Biostatistics to graduate nursing students. She also serves as the State Representative for Ohio’s HD27. In her first year, she sponsored 13 bills addressing topics including adoption modernization, access to MAT for opioid use disorder, Adverse Childhood Experiences, healthcare workplace violence, & childhood exposure to lead. She serves on the Aviation & Aerospace Committee, Behavioral Health Committee, Health Provider Services Committee, Public Health Policy Committee, and Technology & Innovation Committee. She was appointed to the OneOhio Recovery Foundation Board and the Ohio Children’s Trust Fund Board.…

On Research - with CITI Program

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Quality Improvement vs. Research: What's the Difference? - On Research Podcast 36:41

46 weeks 전36:41

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36:41

Join us for a discussion about the always-interesting topic of Quality Improvement vs. Research. What is the difference between QI and Research, and how do researchers and IRBs determine the difference between the two? Tiffany Gommel shares her experience, some helpful insights, and practical advice on this topic. Additional Resources: Example of QI vs Research Checklist from NIH - https://irbo.nih.gov/confluence/download/attachments/70321066/QA-QI%20vs.%20Research.pdf?version=1&modificationDate=1645630780163&api=v2 Example guidance of QI vs Research from Icahn School of Medicine - https://researchroadmap.mssm.edu/other-research/cnri/ebp-qi-research/ Learn more about HRP Consulting here - https://thehrpconsultinggroup.com/ Learn more about CITI Program at about.citiprogram.org . Guest Bio: Tiffany Gommel, the Director of the Office of IRB Operations (IRBO) at the National Institutes of Health (NIH) for the Intramural Research Program, is responsible for the operation and support of the NIH IRB, which reviews and approves human subjects research from the 27 Institutes across the NIH. With over two decades of clinical research experience, Tiffany has valuable expertise running IRBs at multiple organizations.…

On Research - with CITI Program

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The Evolution of IRBs: Navigating Ethical Considerations in Research - On Research Podcast 49:31

51 weeks 전49:31

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49:31

Join us for a thoughtful, long-form discussion about the evolving IRB Industry. Julie Blasingim, the CEO of Univo IRB, sits down to talk about how we got to the current IRB landscape we have now, and the future of IRBs. She covers a lot of areas related to the IRB, including how for-profit IRBs balance ethical reviews with the economics of business, identifying the gap between patients and the IRB process, as well as some hot topics for the IRB, like growing privacy protection concerns and the impact of AI on the IRB process. Additional Resources: Learn more about Univo IRB: https://www.univo-group.com/ NIH article about research populations - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889234/ Learn more about HRP Consulting: https://thehrpconsultinggroup.com/ Learn more about CITI Program at about.citiprogram.org Guest Bio: Julie Blasingim, CEO of Univo IRB, is a seasoned IRB executive with 20 years of extensive regulatory, operational, and compliance experience in human research protection and site operations of clinical research. She has served in a dozen senior leadership roles across multiple central IRBs, has hosted countless FDA inspections at both the IRB and under-site operations, and has managed multiple accreditations and certifications through AAHRPP and ISO. Julie holds a master’s degree in business administration specializing in leadership.…

On Research - with CITI Program

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Improving Access to Research Studies - On Research Podcast 35:31

1 year 전35:31

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35:31

Access to research is a complicated but essential area of growing concern in the research industry. As technology advances, many smaller research sites and rural areas can’t compete or keep up. By narrowing the field of eligible research participants, we lose important patient populations. Jessica Rowe, the Director of Quality and Education at the Yale Cancer Center and the current President of the Society of Clinical Research Professionals (SOCRA), joins me in discussing this fascinating topic. Additional Resources: Resources for increased access to research - https://mrctcenter.org/ Equitable Access to Clinical Trials: How Do We Achieve It? - https://ascopubs.org/doi/10.1200/EDBK_389838 Learn more about the CITI Program at about.citiprogram.org . Guest Bio: Jessica Rowe is the Quality and Education Director for the Yale Cancer Center Clinical Trials Office, where she oversees quality and education initiatives. Throughout her career, Jessica has held varying positions in the clinical research industry, focusing on quality, HRPP, and compliance. She is also the current President of the Society of Clinical Research Associates (SOCRA).…

On Research - with CITI Program

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Navigating the Complexities of Research Security - On Research Podcast 29:54

1 year 전29:54

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29:54

Research security is about protecting the means, know-how, and products of U.S. research and development until they are ready to be shared. In 2021, the government issued a national presidential memorandum with updated requirements for institutions around research. Emily Bradford joins us to explain these new research security requirements and suggests how to grow or build a program to meet these updated requirements. Additional Resources: - The original National Security Presidential Memorandum 33 document: https://trumpwhitehouse.archives.gov/presidential-actions/presidential-memorandum-united-states-government-supported-research-development-national-security-policy/ - National Institute of Standards and Technology – Research Security Framework: https://nvlpubs.nist.gov/nistpubs/ir/2023/NIST.IR.8484.pdf - Updated Policy Regarding Use of Common Disclosure Forms: https://www.whitehouse.gov/wp-content/uploads/2024/02/OSTP-Common-Disclosure-Form-Policy.pdf - CITI Program's Research Security Training Online Course: https://about.citiprogram.org/course/research-security-training/ - Learn more about CITI Program at: about.citiprogram.org . Guest Bio: Dr. Emily Bradford is the Assistant Director of Research Compliance at the University of Kentucky. Under the Office of Sponsored Projects, she oversees conflicts of interest, research security, export controls, and some aspects of clinical trial compliance. She was previously an assistant professor at the College of Medicine and has served on Animal Care and Use Committees as well as healthcare ethics committees.…

On Research - with CITI Program

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Understanding Exception from Informed Consent - On Research Podcast 35:28

1 year 전35:28

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35:28

A growing area of research involves exception from informed consent. In an emergency setting, participants can be enrolled in a trial without their consent. Mike Linke joins On Research to discuss the regulations and ethical considerations around this important area of research. Additional Resources: FDA Guidance Document for EFIC studies - https://www.fda.gov/regulatory-information/search-fda-guidance-documents/exception-informed-consent-requirements-emergency-research NIH Resources about EFIC studies - https://www.ninds.nih.gov/current-research/trans-agency-activities/office-emergency-care-research/research-involving-exception-informed-consent Learn more about CITI Program at about.citiprogram.org Learn more about HRP Consulting at HRP Consulting Group ( thehrpconsultinggroup.com ). Guest Bio: Mike Linke is a scientist, researcher, and IRB Chair. He has been in the research industry for 30 years and serves as the StrokeNet IRB Chair and the SMART IRB Program Director for Education. Mike has extensive experience working with Exception from Informed Consent (EFIC) studies.…

On Research - with CITI Program

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Research Site Operations - On Research Podcast 41:59

1 year 전41:59

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41:59

A discussion about research site operations. We talk about the different types of sites, different recruitment strategies, how DCTs impact dedicated research sites, and the financial impact technology brings to sites. Adam Roth, the Vice President of Site Services at CTI, shares his experience and insights into the site world. Guest Bio: Adam Roth has been in the clinical research industry for over 25 years. He started out as a research coordinator, then manager. He moved into project management at a CRO, then operations director at a central IRB and currently serves as the Vice President, Research Site Services at a phase 1-4 multi-specialty clinical research site. Additional Resources: Interested in participating in a clinical research study? - Sign up with CTI: https://www.ctifacts.com/research-center/participate-in-a-clinical-research-study Developing Clinical Trial Budgets, Considerations, and Best Practices: pharmanewsintel.com Learn more about CITI Program at: about.citiprogram.org .…

On Research - with CITI Program

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Research Compliance - On Research Podcast 31:47

1 year 전31:47

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31:47

Our guest this month is Kate Cohen, the Chief Compliance Officer at SIU Medicine in Illinois. Kate breaks down the concept of research compliance, sharing best practices and practical guidance. We dive into essential elements of a compliance research program, as well as how someone new to this side of the industry can take steps to break in and learn more. Additional Resources: Updated OIG Guidance with 7 Elements https://oig.hhs.gov/compliance/compliance-guidance/ HCCA Conference 2024 Events - hcca-2024-conferences-1pgad.pdf (hcca-info.org) Learn more about CITI Program at about.citiprogram.org…

On Research - with CITI Program

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PRIM&R 2023: Insights and Takeaways - On Research Podcast 29:57

2 years 전29:57

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29:57

This is a special edition of On Research with CITI Program. Guest hosted by Margaret Rankovic, Director of Content and Education at CITI Program, this podcast provides a recap, insights, and key takeaways from the recently concluded PRIM&R 2023 conference. The panel includes the following from CITI Program leadership team: Bharat Krishna, SVP & Managing Director; Jaime Arango, Vice President of Content and Education; Cid Gomes, Senior Director of Information Technology; and Gina Sullivan, Director of Sales and Marketing. The panel shares their personal reflections and observations gained from the conference. Stay tuned to hear about emerging hot topics and key takeaways. We also cover tips for getting the most out of your conference attendance. To learn more about CITI Program please visit: https://about.citiprogram.org/…

On Research - with CITI Program

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Survey Research as a Method: Part 2 - On Research Podcast 24:13

2 years 전24:13

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24:13

Dr. Matt Jans has been conducting and innovating surveys for almost 25 years. He is currently Lead Statistician for the National Health and Nutrition Examination Survey (NHANES) at the National Center for Health Statistics (NCHS).* His survey experience spans academic, government, and private sectors. He is an active member of the American Association for Public Opinion Research (AAPOR). *The views and opinions expressed are those of Dr. Jans and not the Centers for Disease Control and Prevention or the National Center for Health Statistics. Survey research is a dynamic method that transforms curiosity into actionable insights. Utilizing carefully crafted questionnaires, it navigates the intricate terrain of public opinion, illuminating trends and attitudes. A powerful tool in social sciences and business, surveys enable the systematic collection of data, providing a quantitative understanding of diverse subjects. From gauging customer satisfaction to unraveling societal trends, each survey is a snapshot capturing the nuances of human perspectives. Methodical and versatile, survey research is a compass, guiding decision-makers toward informed choices. With its ability to distill complex data into comprehensible patterns, survey research is a cornerstone in evidence-based decision-making. If you found the survey research insights in this episode interesting and want to learn more about this topic, check out CITI Program’s online course, Survey Research: Design, Planning, Implementation, and Ethics, authored by Dr. Matt Jans and Zoe Padgett. This comprehensive resource offers an in-depth exploration of survey research design, implementation, analysis, and ethical considerations. Learn more about CITI Program: - https://about.citiprogram.org/ - https://about.citiprogram.org/course/survey-research-design-planning-implementation-and-ethics/…

On Research - with CITI Program

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Survey Research as a Method: Part 1 - On Research Podcast 14:41

2 years 전14:41

나중에 재생

리스트

14:41

Dr. Matt Jans has been conducting and innovating surveys for almost 25 years. He is currently Lead Statistician for the National Health and Nutrition Examination Survey (NHANES) at the National Center for Health Statistics (NCHS).* His survey experience spans academic, government, and private sectors. He is an active member of the American Association for Public Opinion Research (AAPOR). *The views and opinions expressed are those of Dr. Jans and not the Centers for Disease Control and Prevention or the National Center for Health Statistics. Survey research is a dynamic method that transforms curiosity into actionable insights. Utilizing carefully crafted questionnaires, it navigates the intricate terrain of public opinion, illuminating trends and attitudes. A powerful tool in social sciences and business, surveys enable the systematic collection of data, providing a quantitative understanding of diverse subjects. From gauging customer satisfaction to unraveling societal trends, each survey is a snapshot capturing the nuances of human perspectives. Methodical and versatile, survey research is a compass, guiding decision-makers toward informed choices. With its ability to distill complex data into comprehensible patterns, survey research is a cornerstone in evidence-based decision-making. If you found the survey research insights in this episode interesting and want to learn more about this topic, check out CITI Program’s online course, Survey Research: Design, Planning, Implementation, and Ethics , authored by Dr. Matt Jans and Zoe Padgett. This comprehensive resource offers an in-depth exploration of survey research design, implementation, analysis, and ethical considerations. Learn more about CITI Program: - https://about.citiprogram.org/ - https://about.citiprogram.org/course/survey-research-design-planning-implementation-and-ethics/…

On Research - with CITI Program

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Research and FMLA: Building HR Relationships - On Research Podcast 12:33

2 years 전12:33

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12:33

Tanya Brown is the Senior Director, HR Consulting, Employee and Labor Relations at Vanderbilt University. She has 15 years of experience in Human Resources in many industries including the private sector, public sector, and higher education. Tanya currently leads a team of HR Consultants, who are the primary contact for leaders and employees across the university for matters related to human resources, and workers’ compensation and leave team. Tanya has a Bachelor’s of Arts in Social Sciences with a minor in Psychology from the University of Arizona and a Master’s of Science in Human Resources Strategic Management from Bellevue University. The Family and Medical Leave Act (FMLA) is of paramount importance in a research setting. Researchers often face demanding workloads and unique challenges, and FMLA ensures they can balance their professional commitments with personal needs. This legislation grants eligible employees up to 12 weeks of unpaid, job-protected leave, enabling them to address critical family or health issues without risking their careers. In a research environment, where project continuity is essential, FMLA helps maintain ongoing work, minimizes disruptions, and fosters a more inclusive, supportive atmosphere. It promotes work-life balance, ensuring the well-being and productivity of researchers, thus contributing to the overall success of research endeavors. Learn more about CITI Program: https://about.citiprogram.org/…

On Research - with CITI Program

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Life as an Unaffiliated IRB Member - On Research Podcast 30:10

2 years 전30:10

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리스트

30:10

In this special edition of the On Research with CITI Program podcast, we speak to Sally Mann about her role as an unaffiliated IRB member. Regulations in the U.S. and Canada include requirements associated with the membership of Institutional Review Boards (IRBs)/Research Ethics Boards (REBs). Both regulations require at least one member not to be otherwise affiliated with the institution. Serving as an unaffiliated IRB member is a challenging and rewarding experience. Additional Resources: 45 CFR 46 – Protection of Human Subjects ( https://www.ecfr.gov/on/2018-07-19/title-45/subtitle-A/subchapter-A/part-46 ) TCPS 2 (2002) – Chapter 1: Ethics Framework ( https://ethics.gc.ca/eng/tcps2-eptc2_2022_chapter1-chapitre1.html#a ) CITI Program module - I Have Agreed to be an IRB Community Member, Now What? ( https://about.citiprogram.org/course/biomedical-biomed-basic/ ) Evolving Concern: Protection for Human Subjects ( http://www.youtube.com/watch?v=_8Ku4b1fW18 ) Institutional Review Boards ( http://www.youtube.com/watch?v=U8fme1boEbE )…

On Research - with CITI Program

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Consent in Clinical Research - On Research Podcast 17:46

2 years 전17:46

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리스트

17:46

Linda Reuter has been involved with IRB Administration in various capacities for over 30 years, currently serving as the Sr. Director for BRANY IRB. Responsibilities include supervising the IRB staff, maintaining compliance with the IRB SOPs and applicable regulations, supervising pre and post-IRB meeting activities, expedited reviews, continuing reviews, protocol monitoring, continuing education, development of strategic goals for the organization, maintaining AAHRPP accreditation standards, policy maintenance and development, and training/mentoring of IRB staff. Linda formed IRB Consulting, LLC in 2012, providing IRB administrative services, training and education, audit services, and general consulting to numerous IRB programs nationwide. According to the Food and Drug Administration, the purpose of clinical trials is to study medical products in people. In doing so, consent is critical in clinical trials for these people to understand they are the research subjects and not imply a patient. Consent within research ensures individuals have an informed choice on whether they want to participate in a research study. Informed consent within research is meant to protect human subjects from harm that could occur from participating in research and should always be voluntary. Resources: https://www.niaid.nih.gov/research/dmid-protocols-informed-consent https://www.nsf.gov/bfa/dias/policy/docs/45cfr690.pdf https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980471/ https://www.fda.gov/patients/clinical-trials-what-patients-need-know/informed-consent-clinical-trials…

On Research - with CITI Program

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Consent in Research - On Research Podcast 14:04

2 years 전14:04

나중에 재생

리스트

14:04

Linda Reuter has been involved with IRB Administration in various capacities for over 30 years, currently serving as the Sr. Director for BRANY IRB. Responsibilities include supervising the IRB staff, maintaining compliance with the IRB SOPs and applicable regulations, supervising pre and post-IRB meeting activities, expedited reviews, continuing reviews, protocol monitoring, continuing education, development of strategic goals for the organization, maintaining AAHRPP accreditation standards, policy maintenance and development, and training/mentoring of IRB staff. Linda formed IRB Consulting, LLC in 2012, providing IRB administrative services, training and education, audit services, and general consulting to numerous IRB programs nationwide. Informed consent is critical and a main principle of research ethics in a research study. Consent within research ensures individuals have an informed choice on whether they want to participate in a research study. Informed consent applies to research in the social-behavioral, physical, and medical sciences. Informed consent within research is meant to protect human subjects from harm that could occur from participating in research and should always be voluntary. Learn more about CITI Program: https://about.citiprogram.org/ Resources: https://www.niaid.nih.gov/research/dmid-protocols-informed-consent https://www.nsf.gov/bfa/dias/policy/docs/45cfr690.pdf https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980471/…

On Research - with CITI Program

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Survey Research and Bots - On Research Podcast 19:59

2 years 전19:59

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리스트

19:59

This episode discusses the impact of online bots on survey research, ethical considerations and implications of using bots in survey research, and potential benefits and unintended consequence. Myra Luna-Lucero, EdD, is the Research Compliance Director at Columbia University’s Teachers College. She spearheaded the College’s “Ethics & Safety Amid Uncertainty” initiative and co-chaired the Research Compliance & Safety Committee. She has also recently launched the “Research Writing & Ethics” internship program and oversaw an extensive transformation of the College’s IRB website. She regularly offers seminars and workshops on research compliance and IRB leadership. A researcher and teacher herself, Dr. Luna-Lucero has studied and published on student motivation in STEM fields, barriers to accessing education for students in rural communities, and community activism. Learn more about CITI Program: https://about.citiprogram.org/ Resource: https://www.tc.columbia.edu/institutional-review-board/irb-blog/2022/bots-and-online-human-subjects-research/#:~:text=Researchers%20who%20use%20online%20platforms,posing%20as%20eligible%20human%20participants…

On Research - with CITI Program

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Research Integrity - On Research Podcast 30:41

2 years 전30:41

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리스트

30:41

Ross Hickey is the Assistant Provost for Research Integrity at the University of Southern Maine (USM.) Ross is the Director of the Maine Regulatory Ethics and Training Center (MeRTEC) at USM. He is an attorney in Maine. His office serves institutions throughout the United States. Ross developed and teaches in the Regulatory Ethics undergraduate program at USM. He helped to develop and teaches in the compliance certificate program at Maine Law and also teaches there as an adjunct. He collaborates with universities in the North Atlantic, such as Iceland and Norway. He sits on the World Affairs Council for Maine. Research integrity deals with the “best practices” or rules of professional practice or researchers. The United States National Institutes of Health expands on research integrity by stating it is “the use of honest and verifiable methods in proposing, performing, and evaluating research; reporting research results with particular attention to adherence to rules, regulations, guidelines, and following commonly accepted professional codes or norms.” (From: https://grants.nih.gov/policy/research_integrity/what-is.htm#:~:text=the%20use%20of%20honest%20and,accepted%20professional%20codes%20or%20norms .) Responsible conduct of research (RCR) training is an essential component of any research project, regardless of a researcher’s source of funding. Learn more about CITI Program: https://about.citiprogram.org/…

On Research - with CITI Program

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What is an IRB Administrator- On Research Podcast 17:57

2 years 전17:57

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리스트

17:57

Cecilia Brooke Cholka serves Weill Cornell Medicine as a Human Research and QA Manager and consultant for the PEER Consulting Group. She works to demystify IRB processes and expectations so that researchers and the IRB can work together collaboratively to ensure ethical conduct of research. An Institutional Review Board or IRB is commonly found at institutions that conduct or participate in research activities. The purpose of the IRB is to evaluate research ethics by reviewing research methods related to their potential harm to different groups. An IRB Administrator is an individual who oversees and manages systems, structures, and operations of the IRB related to policy, process, procedures, and records. Learn more about CITI Program: https://about.citiprogram.org/…

On Research - with CITI Program

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Artificial Intelligence in Research - On Research Podcast 21:28

2 years 전21:28

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리스트

21:28

Chirag Shah, Ph.D., is a Professor of Information and Computer Science at the University of Washington. He is the Founding Director of InfoSeeking Lab and Founding Co-Director of the Center for Responsibility in AI Systems & Experiences (RAISE). He works on intelligent information access systems with a focus on fairness and transparency. Artificial intelligence, or AI, is utilized more and more frequently in different settings, including research. AI can be utilized within research by optimizing resources, data, and technology to synthesize and analyze data or problems. With AI in research, so much is still unknown. How do you inform participants of informed consent and protect their data when utilizing AI? How do researchers account for bias or deception while utilizing AI in a research setting? Chirag Shah, Ph.D., discusses these issues and much more on this episode of On Research. Learn more about CITI Program: https://about.citiprogram.org/…

On Research - with CITI Program

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Graduate Research and Controversial Topics - On Research Podcast 12:36

2 years 전12:36

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리스트

12:36

Lou Kavar is a faculty member in psychology at Capella University where he is the lead faculty member for qualitative research and teaches doctoral-level graduate courses in psychology. Lou has taught in higher education at the graduate level for over thirty years. His personal research interest is the integration of spirituality and psychology. He lives in Atlanta, GA. For more information on Lou's writing and work in the area of spirituality, visit his website: loukavar.com. Graduate students at research institutions in the United States are often required to complete a major research project, such as a thesis or dissertation prior to graduation. In these research projects, graduate students might choose to research what one could deem as a controversial topic. Some topics that might be seen as controversial often include topics that involve religion, sex, gender, race, ethnicity, and other topics. Specifically in qualitative research, the researcher should be aware and consider the insider-outsider perspective prior to beginning their research. For graduate students, they should consult with their graduate or research advisor when engaging in research activities involving controversial topics. Learn more about CITI Program: https://about.citiprogram.org/…

On Research - with CITI Program

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What is a Clinical Research Associate? - On Research Podcast 11:44

2 years 전11:44

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리스트

11:44

Elizabeth Waddell, has over 20 years in the clinical research industry and is the owner of The CRA Helper. Elizabeth began her clinical research career as an in-house Clinical Research Associate (CRA) and later transitioned to an on-site CRA. Later in her career, she moved into a Line Manager role that focused on training new CRAs prior to launching her own company, The CRA Helper. What is a Clinical Research Associate (CRA)? A Clinical Research Associate or CRA is a professional within a healthcare setting who oversees research activities, typically related to clinical trials. CRAs can be employed and work in a variety of sectors, including government agencies, pharmaceutical companies, research institutions, and in similar settings. Most CRAs possess an academic degree from a higher education institution in a field related to the healthcare industry. The overall role and tasks of a CRA are outlined and defined by good clinical practice guidelines for clinical trials. Learn more about CITI Program: https://about.citiprogram.org/…