Training Course Description

Mastering the Art of Clinical Trials: Site Selection and Management Excellence for Enhanced Trial Outcomes

Dive into a comprehensive exploration of clinical trial management with our exclusive 2 days, 8-hour webinar training, “Optimizing Clinical Trial Success: Strategic Site Selection, Robust Support, and Effective Management from Inception to Completion.” Developed by a seasoned industry expert with over two decades of hands-on experience in leading biopharmaceutical companies and global CROs, this training offers unparalleled insights into the nuances of clinical trials across all phases of drug development.

Day 1 of our training immerses participants in the critical start-up phase of clinical trials. Delve into the intricacies of strategic site selection, where attendees will master advanced techniques for identifying high-performing sites and principal investigators (PIs) that align with trial objectives and patient demographics. Through interactive sessions and case studies, participants will learn to navigate regulatory landscapes, establish robust infrastructure, and conduct comprehensive site readiness assessments, ensuring sites are primed for efficient participant enrollment.

Transitioning to Day 2, our training delves deeper into recruitment, retention, and ongoing site management strategies essential for sustained trial success. From innovative recruitment tactics to personalized retention initiatives, participants will glean insights into overcoming recruitment challenges and maintaining participant engagement across all phases of the trial. Moreover, our training equips attendees with the skills to effectively manage sites, ensuring compliance, data integrity, and adherence to timelines throughout the trial lifecycle.

Why Attend this Training?

Unlock the keys to success in clinical trial management with a training program designed to meet the evolving demands of the pharmaceutical and clinical research industries. Led by an industry expert with a proven track record of guiding scientific research projects to successful conclusions, this webinar promises to deliver actionable strategies and best practices honed through years of experience. Whether you’re aiming to enhance your skill set, advance your career, or drive operational excellence within your organization, this training offers a pathway to success in the dynamic realm of clinical trials.

By attending this course, you will:

• Master Strategic Site Selection: Acquire advanced techniques for identifying optimal sites and PIs, ensuring swift trial initiation and robust participant enrollment.
• Streamline Site Setup Processes: Navigate regulatory complexities and establish infrastructure conducive to efficient participant enrollment, accelerating trial initiation timelines.
• Enhance Recruitment and Retention: Discover innovative recruitment strategies and personalized retention initiatives to bolster participant engagement and minimize dropout rates across all trial phases.
• Develop Effective Site Management Skills: Gain practical tools and techniques to effectively manage sites, ensuring adherence to compliance standards, data integrity, and operational efficiency throughout the trial lifecycle.

 

 

 

Who should attend?

 

This course is relevant for:

This training is indispensable for professionals involved in drug development and clinical trials execution, including but not limited to:

• Clinical Trials Coordinators
• Clinical Research Associates (CRAs)
• Clinical Trials Operations Managers
• Clinical Research Managers
• Investigators
• Site Coordinators
• Regulatory Affairs Professionals
• Quality Assurance Personnel
• Data Managers

 

 

Whether you’re a seasoned professional seeking to sharpen your skills or a newcomer eager to make an impact in the field, this training provides the essential knowledge and practical insights needed to excel in clinical trial management.

About the trainer

Konstantinos Tsekmes, MSc, MBA –
Associate Director Clinical Operations

Our esteemed trainer brings over two decades of industry expertise, having led clinical studies from phase I to IV, investigator-initiated trials and numerous scientific research projects to successful conclusions.
His expertise spans across various therapeutic areas, including oncology, immunology, infectious diseases, vaccines, general medicine and cardiovascular.
Furthermore, our trainer has spearheaded pre-launch activities for various blockbuster treatments, collaborating closely with internal stakeholders, regulatory bodies, and Key Opinion Leaders.
Renowned for his critical thinking prowess, attention to detail, and unwavering commitment to excellence, our trainer is dedicated to empowering clinical operations professionals with the knowledge, skills, and confidence needed to navigate the complexities of clinical trial management successfully.
With a passion for advancing treatment options and improving patient outcomes, our trainer is committed to driving meaningful impact in the realm of clinical research.