5 Tips for Clinical Trial Managers (CTMs) When Planning for First Site Activated
Planning for the First Site Activated milestone will ensure it is timely and successful. It is best to wait until the protocol is finalized before planning otherwise the milestone may fluctuate. Keep reading for more tips for CTMs planning for First Site Activate
The Importance of the Trial Master File for Each Clinical Trial – and Why Teamwork is Vital
Guest Blog Post - Author Nicole M. Palmer, MS ClinEssentials is grateful to have Nicole Palmer, MS, an experienced Clinical Trial Administrator, Manager, and “Trial Master File (TMF) Enthusiast,” as a guest blogger. Nicole is the CEO of Granular Level, a Trial Master...
How to Get into Clinical Research
If you want to break into the Clinical Research industry, it is helpful to learn the fundamentals and where you can get beneficial experience that will lead you to the best role for you!
How Clinical Trial Managers Are Involved with Study Recruitment
Study recruitment is crucial because a study can only move forward with participants. Finding enough willing and eligible participants can be challenging, depending on the study. That is where a Clinical Trial Manager comes in.
CRA Responsibilities for Each Stage of a Clinical Trial
Most Clinical Research Associates are simultaneously involved with multiple clinical trials, and the typical daily responsibilities differ depending on the stage. Of course, the best CRAs are adept at any clinical trial stage, which comes with experience. Understanding the tasks outlined in this article will help.
How to Review a Clinical Trial Protocol (Free Checklist Included)
The three steps to reviewing a clinical trial protocol are assessing the essential sections, reviewing the entire protocol, and reading the informed consent template. To successfully review a protocol, you must have a list of the crucial sections and take notes throughout your review process.
What is the Difference Between a CRC and a CRA?
CRCs and CRAs work together on a research team, and although their roles sound similar, there are profound differences, including educational requirements, patient involvement, and salary.
Top Organization Tips for Clinical Research Professionals: Organize Your Day & Your “Outlook”
Being organized is vital for maintaining and improving efficiency and productivity when you carry a hefty workload. Begin by organizing your day and your email inbox; we’ve included helpful, doable tips to help you get and keep organized as a Clinical Research professional.
Why Clinical Trials Begin with a Project Kick-Off Meeting (KOM)
The Project Kick-Off Meeting is an essential one-time meeting during which core representatives from the Sponsor and CRO discuss study goals, timelines, and next steps for study activation. The KOM allows the team to meet one another and prepare for a successful trial start.
Conference Call Technology Tips for Clinical Trial Managers (CTMs)
To successfully get through your hours of conference calls, you need to be well-versed on all platforms, prepared with agendas and slide decks, and equipped with a backup plan. You can ensure this happens by being early for your meetings and having technology accessories readily available.
Work-Life Balance for Clinical Trial Managers
The achievement of work-life balance is critical to a Clinical Trial Manager’s ability to consistently deliver high-quality work.
What Does a Clinical Trial Manager Do?
Clinical Trial Managers are in high demand and their role is at the center of every clinical trial. But what do they actually do?