Advanced Site Management: Finance and Productivity Enhanced Business Practices for Clinical Research Programs
AACI’s Clinical Research Initiative (CRI) aims to improve clinical trials management at cancer centers. To help achieve this goal, the CRI annual meeting provides opportunities for clinical trials office administrative directors and staff to share best practices – through peer-to-peer networking, collaboration and ongoing communication – that can lead to more effective cancer treatments.
Learn more about the conference here.
MAGI holds two Clinical Research Conferences per year: one in the Spring in the eastern U.S. and one in the Fall in the western U.S. Our next conference will be in Arlington, VA, May 20-23, 2018, at the Crystal Gateway Marriott. We will then be in San Diego, October 21-24, 2018, at the Hilton Bayfront, and then in Boston, May 5-8, 2019. Hope to see you soon!
Learn how to accelerate your study start-up while maintaining billing compliance, obtaining the required funds for the study, and reducing risk exposure.
Implementing and maintaining effective research administration practices can be difficult for any clinical trials office. Join PFS Clinical for a 1 ½-day workshop to gain valuable insights into all aspects of research administration. This workshop will include speaking sessions by our administration and compliance experts, case studies, and hands-on activities. Topics will include:
Come to Austin, Texas for the primary networking and learning event for compliance and ethics professionals within Research Compliance. Don't miss this opportunity to help increase the effectiveness of your institution's research compliance program by gathering with your peers to discuss emerging risks and issues, share best practices, and build valuable relationships.
Learn more about the conference here.
Clinical Operations & Project Management - Site Management - Regulatory Compliance - Contracts - Budgets
Learn more about the conference here.
Join PFS Clinical for a workshop on research administration!
Learn how to accelerate your study start-up while maintaining billing compliance, obtaining the required funds for the study, and reducing risk exposure.
Implementing and maintaining effective research administration practices can be difficult for any clinical trials office. Join PFS Clinical for a 1 ½-day workshop to gain valuable insights into all aspects of research administration. This workshop will include speaking sessions by our administration and compliance experts, case studies, and hands-on activities. Topics will include:
Learn more about the workshop here!
The annual MEDICAL DEVICE conference, now in its 12th year provides attendees with 2 days of speakers from FDA, site, industry and clinical research/regulatory support organizations.
Learn more about the conference here.
The Society of Clinical Research Associates (SOCRA) recognizes the continuing need for education for Clinical Research Professionals responsible for the activities at the research site or institution. The purpose of this workshop is to assist Research Professionals in improving their skills and their understanding of the responsibilities of conducting oncology clinical research.
Learn more about the conference here.
Bringing together sites, payers, and sponsors to address and discuss clinical billing challenges and best practices to achieve compliance assurance.
Learn more about the conference here.
As the business climate in health care continues to transform, entities engaged in clinical research are evaluating the costs and benefits of participating in clinical research. Is it just about the bottom line in the financial statements? Join PFS Clinical and Bio-Optronics for a webinar to learn about ideas and tips to ensure the mission of the research department/ institute is aligned with the parent organization, and opportunities to communicate value that may not show up in your “P&L Statement”.
Register for this free webinar here!
Join PFS Clinical for a 1 ½-day workshop to gain valuable insights into all aspects of research administration. Topics will include:
Learn more about the workshop here.
As research funds are becoming increasingly competitive, a frequent question asked is, “How much should we pay investigators for their work on a clinical trial and what methodology should be used?”. While the question may seem straightforward, it is far more complex and potentially volatile under the surface. The amount and the method by which you use to pay investigators can play a big role in the success, or lack thereof, of your site.
Join PFS Clinical’s Director of Site Strategy, David B. Russell, for a free, educational webinar on PI Compensation. During this webinar, David will discuss the regulation considerations when setting compensation amounts, the pros and cons of different PI compensation models, and investigator agreement considerations.
Specific areas that will be covered include:
Register here!
Within the past 2 years, interest in investigator-initiated clinical trials has increased greatly. The additional proof of practice and clinical application data that these types of trials provide have allowed for the transition of many newly approved therapies to standard practice.
While research offices are doing their best to support these endeavors, the additional administrative responsibilities involved are often unfamiliar, as they are normally taken on by industry sponsors and outside governmental agencies, including the new “final rule” requirements.
Join Velos and PFS Clinical for an informative, no-cost webinar on investigator-initiated trials and the "final rule" requirements on Thursday, September 14 at 12:00 PM CST. Besides getting tips and models for meeting requirements, learn how technology can help you develop protocols, observe compliance, and simplify submissions to clinicaltrials.gov.
Register here: anymeeting.com/PIID=ED52DE86844C38
Join PFS Clinical For a Webinar on "Investigator Initiated Trials - Administrative Considerations for Successful Study Start-Up and Close Out".
The main points covered in this webinar will be:
This webinar will be hosted by HCCA. Register here.
Research administration is an important part of the clinical trials processes. Developing study budgets, negotiating contracts, and performing coverage analyses are all specialized tasks that require specific training and practice. If done effectively, these processes can save your institution time and money, in addition to ensuring billing compliance. Join research administration experts from PFS Clinical for a 5-part webinar series on the following topics:
This webinar series will be hosted by SCRS. Register here.
Learn more about the conference here.
One of the most important aspects of a clinical trial is a budget that adequately meets the financial needs of your institution; however, in the context of billing compliance, the process of building and negotiating a study budget can become complicated.
In this upcoming webinar, seasoned PFS Clinical staff Amanda Miller and Jill Surfus will review the basics of clinical trial budgeting, provide language tips to prevent potential compliance issues, and discuss how to incorporate a coverage analysis into the budgeting process.
We hope you’ll join us for this complimentary webinar!
Billing compliance is a crucial aspect of any organization that conducts clinical trials. Nonetheless, understanding and applying reimbursement guidelines is one of the most challenging aspects of research. In addition to providing quality patient care, institutions have the added task of understanding and complying with all federal and state guidelines related to clinical research billing practices. These tasks are not only time consuming, but can lead to errors that are costly and could impact your organization’s Medicare standing. Join Senior Clinical Research Analysts Liz Christianson and Nicole Bruecker for a complimentary webinar during which you will learn:
We hope you join us for this informative, no-cost presentation!
Within the past 2 years, interest in investigator-initiated clinical trials has increased greatly. The additional proof of practice and clinical application data that these types of trials provide have allowed for the transition of many newly approved therapies to standard practice.
While research offices are doing their best to support these endeavors, the additional administrative responsibilities involved are often unfamiliar, as they are normally taken on by industry sponsors and outside governmental agencies. Consequently, mistakes made during the initial development and start-up stages of these trials are causing institutions significant financial and compliance-related ramifications.
Join Clinical Research Analyst Liz Christianson as she discusses how to overcome these start-up struggles and oversights of investigator-initiated trials.
Learn more about the conference here. If you're attending, visit us at booth #804!
Learn more about the conference here.