• Entry Level, Intermediate, Senior
• BCO, BD, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, FA, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, , Trainer

Introduction to Decentralized Clinical Trials (DCTs)

Gain the foundational knowledge clinical research professionals need to implement digital health components in clinical trials.

• Entry Level, Intermediate, Senior

Investigational Drug Services Pharmacists: What They Wish You Knew

The Investigational Drug Services (IDS) Pharmacy is not intended to be an impediment to the smooth running of a clinical trial. However, they might see things through a different lens. This presentation will provide insight to the thoughts of an IDS pharmacist. This “inside information” could be quite valuable during site visits and while developing the project itself.

• Entry Level, Intermediate, Senior

How Do IRBs Review Virtual Trial Technology?

Sponsors and investigators are increasingly incorporating mobile medical applications and other virtual trial technologies into their research. Join us for a discussion to better understand the regulations and how the oversight of virtual trials might differ from what they have traditionally been used to.

• Entry Level, Intermediate, Senior

ACRP 2023 Full Program – Replay

A replay package of 62 on-demand session recordings and presentation slides from the ACRP 2023 Conference, April 29 – May 1, Dallas, Texas. It includes content from the five educational tracks, the Signature Series sessions, Rapid-Fire session, and techXpo sessions, presented by a variety of clinical research service providers. Replay sessions will expire on May 31, 2026.

• Entry Level, Intermediate, Senior

ACRP 2023 Workforce Development – Replay

This package is a replay of 8 on-demand session recordings and presentation slides from the Workforce Development Track at the ACRP 2023 Conference, April 29 – May 1, Dallas, Texas. Understand the workforce landscape and gain strategies to build smarter teams.

• Entry Level, Intermediate, Senior

ACRP 2023 Technology & Future Trends – Replay

This package is a replay of 7 on-demand session recordings and presentation slides from the Technology & Future Trends Track at the ACRP 2023 Conference, April 29 – May 1, Dallas, Texas. Gain strategies to optimize technology and move your studies into the future.

• Entry Level, Intermediate, Senior

ACRP 2023 Leadership & Career Growth – Replay

This package is a replay of 10 on-demand session recordings and presentation slides from the Leadership & Career Growth Track at the ACRP 2023 Conference, April 29 – May 1, Dallas, Texas. Get the insights you need to advance your career and grow as a leader.

• Entry Level, Intermediate, Senior

ACRP 2023 Regulatory Trends & Compliance – Replay

This package is a replay of 10 on-demand session recordings and presentation slides from the Regulatory Trends & Compliance Track at the ACRP 2023 Conference, April 29 – May 1, Dallas, Texas. Hear tips and strategies to mitigate risk and keep your studies in compliance.

• Entry Level, Intermediate, Senior

ACRP 2023 Study Management & Conduct – Replay

This package is a replay of 17 on-demand session recordings and presentation slides from the Study Management & Conduct Track at the ACRP 2023 Conference, April 29 – May 1, Dallas, Texas. Learn practical, proven ways to maximize study and site performance.

• Entry Level, Intermediate, Senior

2022 Site Perceptions Industry Survey Results: Actionable Insights for Sites, Sponsors, and CROs

Results of a recent industry survey conducted by the Tufts Center for the Study of Drug Development (CSDD) on site perceptions, preparedness, and experiences with new clinical research execution solutions will be presented. Come see how your experiences compare, and how you can improve site sustainability and lead more effective collaborations. Replay expires June 14, 2026.

• Entry Level, Intermediate, Senior

I Need a Mentor: Where Do I Start?

Join us for a discussion on the value of developing professional relationships in the workplace, and how to differentiate between a network, coach, mentor, and sponsor. Replay expires May 10, 2026.

• Entry Level, Intermediate, Senior

Building a More Equitable Future Together by Driving Inclusion in Clinical Trials

To develop new medicines for everyone who needs them, we must test the safety and efficacy of those medicines on, well, everyone. However, sponsors and sites continue to face challenges as they seek to recruit clinical trial participants that represent the diversity of the people affected by each disease or condition being studied. Sponsored replay expires May 22, 2026.

• Entry Level, Intermediate, Senior

Building Clinical Trial Diversity Action Plans for the Future, Now

Join us as we explore recommended elements of a diversity action plan for research as explained in nonbinding recommendations from the Food and Drug Administration (FDA) released in April 2022. Webinar replay expires March 22, 2026.

• Entry Level, Intermediate, Senior

A Review of ICH E8 (R1) General Considerations for Clinical Trials

Join us for a review of the international harmonized standard for pharmaceuticals used in human clinical studies. Replay expires November 2, 2025.

• Entry Level, Intermediate, Senior

Achieving Global Health Equity Through More Diverse and Inclusive Trials

Join H1 to explore the ABC(and D’s) of clinical trial diversity, equity, access, and inclusion. Replay expires November 16, 2025.

2022 ACRP/Academy Annual Membership Meeting

Join ACRP/Academy leadership to explore highlights of ACRP’s year, learn what’s planned for 2023, and participate in a live Q&A session. Replay expires October 19, 2025.

• Entry Level, Intermediate, Senior

Ensuring Quality in Fast Enrolling Trials

Join us to review a case study from a fast enrolling trial and learn about the strategy to maintain high quality standards. We will discuss and share possible tactics to ensure success when your trial will proceed at break-neck speed. Replay expires September 30, 2025.

• Entry Level, Intermediate, Senior

In the DCT Journey, Every Cloud Has a Silver Lining

Join us as our panel discusses some of the advantages and takeaways learned from the introduction, implementation, and adoption of DCTs. The panel will discuss how they operationalized some of these key takeaways in areas of budgets, contract language, remote monitoring practices, virtual visits, etc. Replay expires September 1, 2025.

• Entry Level, Intermediate, Senior

ICH E9: A Review and a Look Into the Addendum (R1)

Join us for an overview of both the ICH E9 Guideline and the ICH E98 (R1) Addendum. The review will explore how clinical trials are based on statistical principles and how treatment effects are measured in a clinical trial. Replay expires September 1, 2025.

• Entry Level, Intermediate, Senior

Understanding the Role of DMCs and EACs in Research Oversight

Delve into the role and function of Data Monitoring Committees (DMC/DSMB) and Endpoint Adjudication Committees (EAC/CEC) and learn how their oversight is different from the institutional review board (IRB). Replay expires September 1, 2025.

• Entry Level, Intermediate, Senior

Everything You Need to Know About Holding an IND

Join us to review the major responsibilities of holding an Investigational New Drug (IND) application. The presenter will explore common errors and how to avoid these in your trials. Replay expires September 1, 2025.

• Entry Level, Intermediate, Senior

Deconstruct Your Clinical Trial to Plan a Positive Outcome: Effective Planning and Communication Strategies

Join us and learn how to communicate intent and expectations to stakeholders to minimize risk and gain fluidity in operations, along with key elements behind planning a clinical trial and best practices for budgeting a study. Webinar Replay expires August 10, 2025.

Streamline Your Clinical Research Organization’s Processes with End-to-End Promotions

Join Salesforce & FinancialForce for a discussion on how consolidating Discovery, Pre-Clinical, Clinical, and Post Approval processes all on a single platform drives process efficiencies, margin improvement, and real time collaboration internally and with clients. Webinar Replay expires June 29, 2025.

• Entry Level, Intermediate, Senior

Best of ACRP 2022

The “Best of ACRP 2022” package offers recordings from 25 of the most popular sessions from our most recent in-person event, along with seven techXpo sessions, presented by a variety of clinical research service providers.

• Entry Level, Intermediate, Senior

Eliminating Barriers to Careers in Clinical Research

Join Kelly’s talent experts as they discuss the biggest barriers to careers in clinical research and how our profession can remove them to unlock growth in the clinical research workforce. Webinar Replay expires April 23, 2025.

• Entry Level, Intermediate, Senior
• BCO, BD, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, FA, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, , Trainer

The New Work Life Balance in Clinical Research

Join us to gain a virtual toolkit of time management skills that are helpful for navigating the current work environment. Webinar Replay expires February 23, 2025.

• Entry Level, Intermediate, Senior

Virtual ACRP 2021 Full Program Replay

ACRP 2021 programming delivers practical strategies, best practices, and creative solutions needed to improve clinical trial quality.

• Entry Level, Intermediate, Senior

Virtual ACRP 2021 Innovation in the Era of COVID Track Replay

Unlock your potential by learning innovative new ways clinical research is being conducted in response to COVID-19. This online, interactive program addresses telemedicine, remote monitoring, team management, study start-up and more in the era of COVID.

• Entry Level, Intermediate, Senior

Virtual ACRP 2021 Regulatory Trends & Compliance Track Replay

Mitigate risk and improve regulatory compliance with insider advice from FDA officials and industry experts. This online, interactive program features FDA officials and industry experts addressing CDER BIMO compliance and enforcement, FDA inspections, ClinicalTrials.gov requirements, and more.

• Entry Level, Intermediate, Senior

Investigative Site Diversity: Tufts CSDD Study on Staff Diversity at Clinical Research Sites

Join us as the Tufts CSDD team shares their survey results around staff diversity at clinical research sites. Webinar Replay Expires December 15, 2024.

The Push for Technology: A Discussion of Implementation Struggles, Strategies, and Lessons Learned

Join us for a panel discussion on how the pandemic pushed the implementation of technology for some sites. Replay expires December 16, 2024.

Best Practices for Communicating Benefit, Risk, and Uncertainty in Medical Device Clinical Trials

Learn the evidence-based practices for communicating the benefits, risks, and uncertainty regarding medical technology to patients and providers. Replay expires December 16, 2024.

Using Agile Strategies to Solve Challenges in Research Operations

Learn how to move at the rate and pace you need to within your research infrastructure to advance, innovate, and improve. This Webinar Replay expires December 8, 2024.

• Entry Level, Intermediate, Senior

Virtual ACRP 2021 Operational Efficiencies Track Replay

Boost efficiency in clinical trial management and execution with practical strategies for sites, sponsors, and CROs. This online, interactive program addresses collaboration, protocol feasibility, decentralized trials, remote monitoring, and more.

Clinical Research Staffing Reprioritizations and Resourcing Strategies

Join us to discuss results from the Advarra Trend Report: The Future of Work in Clinical Research and learn when to look for help and when to change your staffing approach. This Webinar Replay expires November 9, 2024.

The Future of DCTs: Are You Prepared?

Session Replay Expires November 3, 2024 — Join us to learn how to make sense of DCTs relative to your career path and get a tool kit to position yourself for success.

techXpo Replay—Research Ready: Leveraging Technology in the New Research Landscape

Replay expires October 8, 2024 — Join Advarra experts in a discussion on how to leverage technology in the new research landscape

techXpo Replay—Working with Site-Based Paperless Solutions and Ensuring Audit Readiness

Replay expires October 8, 2024 — Join RealTime experts for an overview of site-based electronic systems that the research industry is rapidly adopting.

techXpo Replay—Achieving Regulatory Compliance via Collaboration: Technology and Site Perspectives

Replay expires October 8, 2024 — Join experts from WCG Velos and the University of Kansas Medical Center to learn top practices and processes sites follow to meet compliance standards.

Communication Strategies for Conflict Resolution in Clinical Research Teams

Replay expires August 25, 2024 — Join us to examine how specific communication behaviors can foster effective conflict resolution that facilitates team growth.

Career Paths in Clinical Research: Sharing the Journey and Providing Insight

Replay expires August 18, 2024 — Join our panel of clinical research professionals as they discuss their career paths into and through the clinical research industry, how they see the future of their roles, and what advice they would give to those wanting to join the industry.

Let’s Talk Patient Recruitment: Strategies, Tools, Communication

Replay expires July 14, 2024 — Join ACRP Editor-in-Chief, Michael Causey, as he reviews two recruitment strategies with our guests that have helped increase efficiencies and increase patient recruitment into trials.

Clinical Trial Diversity: Strategies to Support Patients, Sites, and Sponsors

Join executives from Merck Research Laboratories to explore practical strategies for engaging and enrolling diverse patients in clinical trials.

Monitoring Investigator-Initiated Trials

Explore the processes and procedures needed to design and implement a monitoring program for investigator-initiated research studies, with a specific focus on sponsor-investigator studies that involve an Investigational New Drug or Investigational Device Exemption.

Improving Technology Proficiency in Clinical Research

Join Veeva Systems to explore what a competency-based approach to technology looks like in clinical research.

techXpo Replay—How to Build Advanced Workflows with an Integrated Technology Environment

Join Florence Healthcare to learn how to harness the power of best-in-class software while avoiding digital fatigue, duplication, and wasted time.

techXpo Replay—Quality Improvements as a Result of Paperless Site-Based Systems

Join RealTime CTMS to examine how paperless sites and site networks are driving quality and improved timelines for the clinical research industry.

techXpo Replay—Exit the Feature Battle: How to Think Long Term and Prepare Your Site for the Future of Technology in Clinical Research

Join Veeva Systems to explore the key qualities and features sites need to look for in their technology partners to increase their connectivity with sponsors and patients.

Research and Expanded Access in Pandemic Times

Explore the mechanisms allowing experimental COVID-19 therapies and diagnostics to patients and how that has affected researchers’ ability to generate substantial evidence of product effectiveness.

Good Clinical Practice (GCP) Simulation

The New Standard in GCP Training. This interactive simulation-powered training course helps ensure compliance with international standards for Good Clinical Practice in clinical trials (ICH E6).

techXpo Replay—COVID Catch 22 – Don’t Get Burned Out by Dependency on Technology

Ready to simplify your technology footprint for 2021? Join Exostar to explore how to streamline technology access and create a better user experience.

techXpo Replay—eSource: Why This is the Platform of the Future

Join experts from Clinical Research IO to explore how several independent trends in research will make eSource a platform technology for sites.

techXpo Replay—The Impact of Brexit and COVID-19 on Clinical Research Data Processing in the EU/UK

Join The DPO Centre for this exploration of data protection challenges relating to the handling of sensitive personal data of EU and UK trial participants and how COVID-19 has bought data protection to the forefront of people’s minds.

techXpo—COVID Catch 22 – Don’t Get Burned Out by Dependency on Technology

January 14, 2021 1:30-2:30 PM ET – Ready to simplify your technology footprint for 2021? Join Exostar to explore how to streamline technology access and create a better user experience.

Continuing Organizational SOP Needs to Maintain Compliance (Session I)

Join us for part one of the Webinar series ‘Adaptive Operational Optimization through Transformative SOPs’ and learn to transform operational effectiveness by drafting your clinical research SOPs to be specific, meaningful, and productive for your unique organization.

Transforming SOP Infrastructure for COVID Times (Session II)

Join us for part two of the Webinar series ‘Adaptive Operational Optimization through Transformative SOPs’ and explore the stages of the SOP life cycle beyond merely drafting to include training and enforcement as well.

SARS-Cov-2, the Law, and You

This ACRP / SCRS webinar replay discussed how COVID-19 laws and regulations affect small clinical research sites.

COVID-19 Technology Mad-Dash, What Worked and What Didn’t?

This Webinar will address the challenge of transforming clinical research operations with technology built from the rapid transformation clinical research sites had to undergo in light of COVID-19 disruptions.

Innovative Approach of Using EHR Data to Improve the Speed, Efficiency, Quality and Costs of Conducting Clinical Trials

Learn how a research site’s electronic health record (EHR) data can be used to precisely identify potential subjects from their patient population, reducing the recruitment and screening effort and accelerating the time to completion of enrollment.

Practical Tips for Career Development

Learn to build a successful career for yourself all while developing a strong team, by understanding different personality types and how to communicate with them.

Building Relationships With Healthcare Professionals and Community Groups to Increase Enrollment

Join us as we explore best practices for building and maintaining relationships with healthcare professionals and community groups in order to increase study enrollment, especially among diverse populations.

techXpo Replay—GDPR for Clinical Research Professionals: Handling EU and UK Medical Data in a Post Brexit World

Join The DPO Centre to explore data protection challenges and solutions when handling the sensitive personal data of EU and UK trial participants.

techXpo Replay—Increase Efficiency and Accelerate Trial Timelines with eISF and SSO, presented by Exostar & Cognizant SIP

Join Exostar and Cognizant for an informative session on improving trial efficiency through SSO and eISF.

techXpo Replay—Going Digital: How Sites are Moving Research Forward During a Pandemic

Join Veeva Systems to learn how COVID-19 has resulted in greater need to keep existing clinical trials on track by enabling digital processes and remote access for study monitors.

techXpo Replay—Knowing is Half the Battle: How Site Performance Reports Can Optimize Clinical Trial Outcomes and Strengthen Partnerships

Join Merck & Co. for a session examining the benefits of site performance reports from the perspective of both a Sponsor/CRO and a site.

Diversity of Research Personnel: Knowing Who We Are to Know Who We Serve

Evaluating recruitment efforts to increase diversity among subjects to make research findings more generalizable and applicable to all populations.

techXpo Replay—Dismantling the Status Quo of Monitoring: Moving Towards a Technology-Enabled Approach to Trial Oversight

Join Remarque for a session discussing leveraging technology to allow for more efficient monitoring.

techXpo Replay—Disrupting the Clinical Research Market: Leveraging Innovative Approaches and Technologies from Other Industries

Join Schlesinger Clinical Research as they share best practices that will improve your studies.

techXpo Replay: Virtual Site Monitoring: The Evolution of Remote Site Monitoring

Join VirTrial and Florence Healthcare for a session discussing the current and future state of clinical trial monitoring.

techXpo Replay: A Two-Step Approach to Improving Patient Recruitment

Join Ripple Science for an informative session centered around the effectiveness of centralized recruiting models against standardized models.

Informed Consent Simulation

This interactive, simulation-powered training program helps ensure informed consent is obtained by the right subject, with the right forms, by the right people, through the right process, at the right time, and with the right documentation.

ACRP Clinical Research Knowledge Assessment™ (CRKA)

Whether you’re an emerging professional looking to demonstrate your foundational knowledge to prospective employers or an organizational leader looking for an efficient, effective way to vet new hires, ACRP’s new Entry-Level Knowledge Assessment (ELKA) is for you.

Certified Quality Manager Training

Increase your influence and expand your career opportunities by validating your commitment to quality. The Quality Management Institute and ACRP have partnered in a program of education for individual professionalism and the quality management of clinical research sites.

• Entry Level, Intermediate, Senior
• BCO, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, PMs, QCS, RS, RM, RTA, SSSU, Statistician, , Trainer

Clinical Trial Monitoring Basics

Become an expert on quality and risk-management strategies and procedures. This interactive eLearning course answers the fundamental questions: What is RBM and how is it different from the standard monitoring approach?

• Entry Level, Intermediate
• BCO, BD, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, FA, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, , Trainer

Ethics and Human Subject Protection: A Refresher Course

When in need of a comprehensive refresher, this on-demand eLearning course provides a consolidated overview on the history and importance of ethical conduct in clinical trials involving human subjects.

• Entry Level
• Investigator,

Investigator Responsibilities

Learn the various responsibilities of clinical investigators based on FDA Regulations, ICH Guidance Documents, and international standards.

• Senior

Improving Recruitment, Accrual, and Retention in Clinical Trials

Explore best practices to improve recruitment and retention with a focus on operational efficiency, cultural competency, and patient centricity. Included tools will help you assess how to better communicate with potential participants and begin a critical reflection of your own skills and organizational practices.

• Senior

Trial Feasibility and Selection: Their Impact on Accrual

Selecting the right trial for your clinical research site is key to the success of your accrual for the trial. This eLearning course will discuss how the menu or portfolio of studies offered at a site has an important impact on accrual and how research professionals can become part of the process.

• Entry Level
• CRC, CRN, Investigator, PR, RM

Implementing a Patient-Centered Informed Consent Process

Improve your consent process by learning how to assess a participant’s reading level, health literacy, and overall understanding of clinical trial participation and address culture, learning styles, emotional states and language. This eLearning course will provide essential tools for those directly involved in informed consent discussions.

• Intermediate
• CRC, CRN, Investigator, PR, RM

Using Metrics to Improve Subject Recruitment and Retention

Overcome challenges in subject recruitment and retention by learning how to leverage the metrics critical to success. This eLearning course will teach site personnel assess current site performance and readiness for action, and to implement appropriate metric measurement and monitoring.

• Entry Level
• BCO, BD, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, FA, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, Trainer

Introduction to Clinical Trials

Fundamental education about the role clinical research plays in advancing medical knowledge and the work conducted by clinical research professionals. This free eLearning course details how medical products are developed, how volunteer patients are protected, and key roles in the development, research, review, and approval of medical products.

• Intermediate, Senior

Site Quality Management Tools: SOPs, Metrics and Training

Master quality-related processes and procedures required to ensure trial compliance. This eLearning course is a comprehensive training program that prepares you for the next step of setting up a quality management system– essential information for site personnel involved in quality management and improvement.

• Entry Level, Intermediate, Senior
• BCO, CDC, CRC, CRN, CRS, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, Trainer

Inspection Readiness: Best Practices for Managing Clinical Trial Inspections

Reduce your anxiety by being prepared for clinical trial inspections. This eLearning course takes you through the full cycle of a regulatory authority GCP inspection and answers key questions including: Why, when and where are regulatory inspections performed? Who can be inspected? And more.

• Entry Level, Intermediate, Senior
• BCO, BD, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, FA, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, Trainer

Mastering the Event Reporting Cycle: Understanding Your Impact on Patient Safety

Efficiently identify and report safety events in your clinical trials. This eLearning course, appropriate for all clinical research professionals, guides you through the complete event reporting cycle and critical timelines, as defined in ICH E2a and E6 Guidelines.

• Entry Level, Intermediate
• BCO, BD, CDC, CRC, CRN, CRS, DM, Investigator, MA, MD, MRS, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, Trainer

Understanding Clinical Trial Protocols: Key Considerations for Effective Development and Feasibility Review

Expand your knowledge and skills in study protocol design and review. This e-Learning course covers the anatomy of a protocol, hypothesis development, study design, subject safety and data integrity risk considerations, protocol feasibility and protocol amendments.

• Entry Level, Intermediate, Senior
• BCO, BD, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, FA, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, Trainer

Statistical Principles for Clinical Trials: Overview of ICH E9

Improve protocol interpretation and implementation by understanding trial scope, design, conduct, data analysis, and the evaluation and reporting of safety and tolerability data. This eLearning course explores the International Conference on Harmonization’s E9 guideline Statistical Principles for Clinical Trials.

• Entry Level
• BCO, CRC, CRN, DMCTO, Executive, FA, Investigator, MCRA, PMs, RM, RTA, SSSU, Trainer

Mastering Budgeting at Your Site: Building and Negotiating Clinical Trial Budgets that Make Sense

An essential course for all clinical research professionals involved in the clinical trial agreement and/or budget process for industry-initiated trials.

• Intermediate, Senior
• BCO, BD, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, FA, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, Trainer

Key Skills for Ensuring Quality Control through Risk-Based Decision Making

Gain confidence in making risk-based decisions and implementing actions related to quality control initiatives. This eLearning course covers key aspects related to risks in clinical trials, including: identification, analysis, planning, communication, change management and much more.

• Intermediate, Senior
• CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, Trainer

ICH Gap Analysis

Assess your and your team’s training needs quickly by conducting an ICH gap analysis. This eLearning course uses a game to challenge the learner’s knowledge and application of these important efficacy guidelines.

• Entry Level, Intermediate, Senior
• Investigator, MCRA, PMs

Form FDA 1572: Get it Right the First Time

The Statement of Investigator (Form FDA 1572) doesn’t have to be complicated – let us help you get it right the first time. This eLearning course answers the questions of why, when and how to complete the FDA 1572 to make everyone’s jobs easier.

• Entry Level
• BCO, BD, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, FA, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, Trainer

Ethics and Human Subject Protection: A Comprehensive Introduction

Explore the ethical considerations facing clinical research professionals and learn to put the rules into practice to ensure human subject safety and well-being. This eLearning course provides in-depth training on the importance of ethical conduct in clinical trials involving human subjects.

• Entry Level, Intermediate, Senior
• BCO, BD, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, FA, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, Trainer

The Drug Development Process: ICH E8(R1) General Considerations for Clinical Trials

Develop a better understanding of the overall drug development process and how each study fits into the “big picture” of the development life cycle. This eLearning course puts into practice the ICH E8 guidance document General Considerations for Clinical Trials.

• Entry Level, Intermediate, Senior
• BCO, BD, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, FA, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, Trainer

Building Quality Management Systems for Sites and Sponsors: Root Cause and CAPA

Implement a Quality Management System (QMS) and prevent findings related to patient safety, data quality and regulatory compliance. This eLearning course will teach you risk management strategies to avoid inaccurate trial data, regulatory non-compliance and more.

• Entry Level, Intermediate, Senior
• BCO, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, Investigator, MA, MD, MRS, MSO, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Trainer

eResearch: Managing Clinical Trials in an Electronic Environment

Learn how to set up and manage electronic clinical research documents in compliance with U.S. and EU regulations, and current trends from both the site and sponsor perspectives. This eLearning course examines the challenges of working with electronic documents and how to overcome them.