17th Annual Optimising Clinical Trials Summit: Site Selection, Feasibility and Patient Recruitment

Embark on a remarkable journey of discovery and innovation at the 17th Annual Optimising Clinical Trials Summit: Site Selection, Feasibility & Patient Recruitment. Prepare to be captivated as we explore the theme of patient-centred trials, where groundbreaking ideas and transformative strategies take centre stage; unlock the clinical data`s power to shape the very future of clinical trials; delve into the designing randomised controlled trials, where best practices intertwine with cutting-edge innovations; expand your horizons with patient recruitment; uncover strategies to foster engagement and ensure a diverse and inclusive participant pool; witness firsthand the impact of these optimisations as patient-centred Trials flourish, empowering individuals and revolutionising the healthcare landscape.

We create an atmosphere of friendship, innovation, and collaboration. Additionally, we provide networking opportunities with esteemed professionals, forging lasting connections that will propel your career forward. Immerse yourself in a vibrant tapestry of knowledge-sharing, where ideas flourish and boundaries fade away.

The 17th Annual Optimising Clinical Trials Summit promises to be an extraordinary event where minds converge, ideas take flight, and the future of clinical trials is reshaped. We eagerly anticipate your presence as we collectively redefine what is possible and revolutionise the realm of clinical trials.

Join us and register today

Stay on top of the latest trends

Key speakers

Marta Garcia Manrique

Marta Garcia Manrique

R&D. Chief Patient Office
Regine Buffels

Regine Buffels

Global Medical Director
Maarten Boomsma

Maarten Boomsma

Clinical Research Director
Jose Manuel Cervera-Grau

Jose Manuel Cervera-Grau

Executive Director Clinical Oncology
Joachim Luithle

Joachim Luithle

Senior Vice President, Head Clinical Operations

Key topics

  • Advancing patient-centred trials: How to leverage innovations and technologies?
  • Unlock the power of the clinical data: Shaping the future of clinical trials
  • Designing randomised controlled trials: Best practices and innovations
  • Expanding the pool of engaged patients: Optimisation of patient recruitment
  • The roles and responsibilities of stakeholders in the sharing of clinical trial information
  • Regulations on clinical trials: The influence that will shape medical affairs

Who Should Attend

Members of board, C-level, Senior/Global Vice Presidents, Directors, Heads of departments from the pharma industry involved in:

  • Clinical Trials
  • Clinical Operations
  • Clinical Information
  • Clinical Development
  • Outsourced Trials
  • Decentralised Trials
  • Hybrid Trials
  • Virtual Trials
  • Randomized Trials
  • Trial Management
  • Clinical Study
  • Safety Science
  • Site Intelligence
  • Patient Centricity
  • Data Scientists
  • Clinical Innovations
  • Site Management
  • Clinical Management
  • Clinical Research
  • Global Safety
  • Risk Monitoring
  • Data Integrity
  • Feasibility
  • Patient Recruitment