Top Trial Master File Best Practices for CRAs: Expert Insights and Tips

Hey TMF Daily enthusiasts! Welcome back to another power-packed episode. Today, we're diving deep into the pivotal role of the Clinical Research Associate (CRA) in the Trial Master File. Whether you're an eTMF Specialist or a Clinical Trial Assistant, this episode is a must-listen as we uncover the crucial responsibilities and interactions of CRAs.

Here's what we'll be breaking down:

*The essential documents you need at a Site Initiation Visit (SIV)

*The critical details CRAs look for in the Delegation of Authority (DOA) log

*Six essential steps that CRAs follow during a Monitoring Visit

Joining us is the incredible Maria Alexander Milas. Maria holds a Master’s Degree in Clinical Trial Monitoring, is a Certified Clinical Research Professional (CCRA), and has extensive experience in clinical operations spanning both CROs and sponsors.

So get ready for an episode packed with actionable tips and career-changing insights for all you CRAs and clinical research professionals out there.

Don’t forget to subscribe, share, and leave us a review. Until next time, keep pushing boundaries and mastering your TMF!

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Enjoy the show! #clinicalresearch #trialmasterfile #clinicaltrials