How to achieve successful clinical trial recruitment

This course focuses on the crucial aspects of successful clinical trial recruitment. It covers protocol and site feasibility, recruitment timelines, risk mitigation, and strategies for improvement.

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Course Overview

This course focuses on the crucial aspects of successful clinical trial recruitment. It covers protocol and site feasibility, recruitment timelines, risk mitigation, and strategies for improvement. Participants will learn how to plan effectively, calculate recruitment, identify risks, and develop mitigation strategies. The course is ideal for clinical research managers, project managers, lead clinical research associates, and any clinical function impacted by study recruitment.

Key Topics

We, at Wehive, offer you in-house training programmes conducted by inspiring coaches that are
Introduction
Protocol feasibility
Site feasibility tips and tricks
Timelines and recruitment calculations
Clinical trial advertisement considerations
How to improve recruitment during your study
Round table / workshop

Learning Objectives

  • Being able to plan a good protocol and site feasibility to select the best centres
  • Describe how to calculate recruitment and timelines
  • Identify risks associated with study participants recruitment in a clinical trial
  • Describe risk mitigation strategy to ensure successful recruitment

Who Should Attend?

An event precisely for you
  • Any clinical function impacted by study recruitment as Clinical Research Managers and Project Managers, (Lead) Clinical Research Associates (CRAs), etc.

Meet Your Trainer

With a master’s in chemistry Nelle Stocquart works since 2003 in the Clinical Research world. She was first an IVRS project manager for a Belgian CRO but then she wished gaining more experience on the field and became CRA for a top 5 international CRO where she got involved in many international phases II & III from early study stage till closure.

She then evolved as project manager in pharmaceutical companies and CRO where she managed local and international studies from phase I to phase IV. She is now working for the Belgian government which is funding academic studies. Nelle has a lot of experience in project management, team management and people coaching. Training, Coaching, Education and Continuous Professional Development have always been the common pillars in her educational path and professional career. She speaks fluently 3 languages (Dutch, French and English).

Her real passions are “technical skills”-trainings:  

-Project Management 
-Risk Management 
-Risk Based Monitoring 
-CRO Selection and Management 
-Time Management 
-Clinical trial budget management 
-Advanced Project Management 

She provides standardized training, but also tailor made sessions adapted to the specific needs of the client and the company. 

Nelle Stocquart

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