Q&A Part II: Developing Leaders and Building Successful Careers in Your Organization
In this Part II Q&A, Dr. Suzanne Rose answers additional attendee questions from her webinar “Developing Leaders and Building Successful Careers in your Organization.”
Q&A Part I: Developing Leaders and Building Successful Careers in Your Organization
In this Q&A, Dr. Suzanne Rose answers attendee questions from her webinar “Developing Leaders and Building Successful Careers in your Organization.”
Paying Research Volunteers: How to be Participant-Centric
Does your payment process follow these guidelines?
Study Activation: A Complex Process That Doesn’t Have to Be Painful
Long activations is a familiar concept in the clinical trial landscape. How can your site improve your study activation timelines?
IRB Review of Coronavirus and Other Emerging Infectious Diseases: Issues to Consider
There are unique issues that research involving emerging infectious diseases like coronavirus can raise for IRB review and research informed consent.
Making the Most Out of Your Next Clinical Research Industry Conference
Attending an industry conference reaps many benefits, but you get out of it what you put into it. Check out these tips and tricks to maximize your time.
How Staff Augmentation Services Help Accelerate Project Timelines
When a customer wanted to implement OnCore and Forte eReg, they knew they didn’t have the staff resources to start the project right away. They chose Staff Augmentation services to help jump start their project.
How Technology and System Integration Can Improve Your Billing Compliance
Choosing the right CTMS can enhance your billing compliance and minimize risk.
Preview: Forte’s Pre-Conference Workshop at CCAF 2020
At this year’s CCAF conference, we will host a pre-conference workshop, “Research Administration Technology Workshop”, allowing us to work collaboratively with the clinical research community.