Discover an informative webinar that dives into the critical role of efficient study start-up processes in the rapidly evolving landscape of clinical research.
In the rapidly evolving landscape of clinical research, the speed and efficiency of study start-up processes are crucial for accelerating the development of new therapies and interventions.
In this webinar, the expert speakers will discuss innovative strategies and practical solutions to streamline the study start-up phase from protocol feasibility assessments to regulatory submissions and site activation. They will share real-world examples and case studies while discussing how to overcome common challenges, reduce time-to-initiation and ensure smooth collaboration between sponsors, Contract Research Organizations (CROs) and sites.
The attendees will gain comprehensive insights into the challenges typically encountered during the study start-up phase of clinical trials and obtain practical solutions to address these obstacles. They will learn about the advantages of implementing centralized and standardized procedures within a clinical site network, which can considerably streamline processes and improve efficiency.
The speakers will also delve into effective communication strategies that are essential for ensuring seamless coordination among all stakeholders involved in clinical trials. This webinar is ideal for clinical trial professionals looking to enhance their understanding of study start-up processes and improve their ability to execute clinical trials efficiently.
Register for this webinar today to gain insights into the critical role of efficient study start-up processes in running clinical trials for the development of new therapies and interventions.
Speakers
Jack Evans, Vice President, Site Operations, EmVenio Research
Jack Evans has over a decade of clinical research experience that spans over 5 continents and is knowledgeable in a vast array of therapeutic areas and trial designs across all phases of clinical development. As Vice President of Site Operations at EmVenio, he is focused on developing infrastructure, client partnerships and leading operational delivery to grow businesses.
Jack has held senior positions at Pratia, PPD (AES) and Synexus Clinical Research. A cross-functional and operational delivery leader, he was part of the team that built Europe’s largest site network, implemented international feasibility, contracts and global projects. He earned a BS in Pharmaceutical Science from the University of Wolverhampton, Faculty of Science & Engineering.
Message Presenter
Tara Kidwell, Sr. Director, Global Project Management, EmVenio Research
With over a decade of experience in project management and a proven track record of leading global teams, Tara Kidwell is a dynamic and results-driven professional. As the Senior Director of Global Project Management at EmVenio, Tara excels in orchestrating complex projects, driving strategic initiatives and fostering cross-functional collaboration.
Her expertise spans clinical research, operational excellence and innovative problem-solving. Prior to EmVenio, she was at Matrix Medical Network where she was responsible for the Global Project Portfolio and supported the build of a novel mobile site network across the US.
While at Matrix Tara, she served in several different roles in operations spanning across three different business lines: employee health and wellness, clinical trials and clinical care home visits. Tara earned a BS in Criminal Justice at the University of Alabama at Birmingham.
Message PresenterWho Should Attend?
This webinar is ideal for any sponsor, CRO or clinical research professional interested in learning more about localized clinical trial options:
- C-suite in Clinical trial management
- Innovation/Therapeutic Lead/Head
- Clinical development/operations/trial feasibility
- Clinical Risk Manager
- Medical/Operational Director
- Patient advocacy/engagement
- Project management
- Site selection/feasibility
What You Will Learn
Attendees will learn about:
- The typical obstacles faced during the study start-up phase and practical solutions to address them
- The benefits of centralized and standardized procedures within a clinical site network
- Effective communication strategies to ensure seamless coordination among stakeholders
- Real-world examples of successful study start-ups
Xtalks Partner
EmVenio Research
EmVenio Research, a PCM Trials Company, provides a scalable network of clinical trial sites strategically located in underrepresented communities to engage a diverse patient demographic. Our extensive global network comprises highly skilled clinicians, leading principal investigators, and cutting-edge research sites, allowing us to deliver high-quality clinical research services that prioritize reducing the burden on patient participation.
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