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Conference Overview

The Global Clinical Trials Connect 2023 will provide a platform to discuss on the futuristic advancements in clinical trials and clinical research. This multidisciplinary program involves broad participation of people from clinical trials community from around the globe who are focused on learning more about clinical research, clinical trials planning and management.

 

The Pharma and Bio-Tech companies are consistently evolving and new clinical studies, technologies and advancements in care and treatments have augmented the efficiency and at the same time the complexity of clinical trials has increased, with tests being carried out in a highly structured and closely coordinated manner. It is high time that we look into innovative strategies, new technologies, effective and quality collaborations to address these issues, which can cater to the needs of the patient and the industry.

 

This conference intends to focus on the global health and clinical trials around the world. Bioethics, regulations, patient recruitment, site selection, real-world data, data integration & Strategy, outsourcing, vendor management, quality (QbD) in Trial Conduct, risk-based monitoring, clinical auditing & financial planning and other significant topics that play a key role in clinical trials will be addressed along with innovative sessions on new technologies, effective and quality collaborations.

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This program will certainly educate health care scientists on trial design, operations, organizing trials, research computing, regulatory aspects, report on clinical trials and gain a better knowledge of the implications of clinical trials in prevention, diagnosis, clinical trial-related ethics and disease treatments.

 

The summit will facilitate an invaluable networking opportunities with decision makers and focus on real case studies, insightful presentations and round tables.

 

It gives us a great pleasure in welcoming you to the Global Clinical Trials Connect 2023.

 


KEY HIGHLIGHTS

  • Patient Recruitment and Site selection
  • Innovative trial designs
  • Partnership & Collaboration - Sponsors, CROs, Sites and External Vendors
  • Patient centric clinical trials
  • Making Patient Engagement a Reality
  • New innovations in Patient Recruitment planning and execution on a clinical trial
  • Outsourcing strategies and models
  • Electronic Clinical Outcome Assessment and Electronic Patient Reported Outcome
  • Streamlined IRT development process
  • Pharmacovigilance & Clinical Trials
  • Post-Clinical Trial closed communities
  • How to future proof your clinical operations
  • Diversity and Inclusion in Clinical Trials
  • Implementing Risk Based Monitoring
  • Streamlining R&D and lower costs in clinical trials
  • Adaptive Trial Model
  • Clinical Trial Auditing
  • Real World Clinical Trial Strategies
  • Data Quality & Technology
  • Clinical Data Strategy & Analytics
  • Electronic Data Capture (EDC) Systems
  • Decentralised Clinical Trials
  • Clinical Technology and Driving Innovation
  • M-Health, Wearable and Consumer Technology
  • Big-Data, IoT and Artificial Intelligence in Clinical trials
  • Blockchain technology for improving clinical research quality

 


WHO SHOULD ATTEND THE CONFERENCE

 

This event is designed for senior level attendees from various companies including Pharmaceutical, Bio-Tech, Bio-Pharma, CRO’s, Investigative Sites, Solution provider and Government institutions.

 

Attendees includes VPs, GMs, Directors, Heads and Managers of

  • Clinical Trials
  • Clinical Study Management
  • Clinical Operations
  • Clinical Research
  • Patient Organizations
  • Patient Recruitment
  • Outsourcing
  • Vendor Management
  • Site Management
  • Site Monitoring
  • Clinical Pharmacology
  • Clinical Data Management
  • Risk Monitoring
  • EDC
  • Clinical/Digital Innovation
  • Clinical Design/Protocol design/ Strategy makers
  • Clinical Research Sites
  • CROs and CMOs
  • Hospitals/ Associations
  • Regulatory affairs 

 

 

 

 

pharmaceutical companies

Speakers

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There are plenty of opportunities to position yourself as a thought leader & showcase your company.

For enquiries on speaker opportunities please e-mail to speaker@corvusglobalevents.com

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Wednesday - 10th May 2023

  • 08:00

  • Registration & Refreshments

  • 08:50

  • Chairperson’s opening remarks

    Nancy Meyerson-Hess

    Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
     eMQT

  • 09:00

  • DCT Case Studies – Real World Learnings from DCTs in Europe and the US

      Presentation
    Rebecca Jackson

    Rebecca Jackson Sr. Mgr. Clinical R&D Innovation & Novel Modalities IT
     The Janssen Pharmaceutical Companies of Johnson & Johnson

  • 09:30

  • Clinical Trial Decentralisation: Why Implementation Matters?

    • The DCT framework
    • How to ensure appropriate standards and protocols in a decentralised clinical trial environment
    • Potential barriers to the adoption of decentralised clinical trials and how to overcome them
      Presentation
    Nikita Sharma

    Nikita Sharma Global Clinical Sciences & Operations Innovation Manager
     UCB

  • 10:00

  • Decentralized clinical Trials- An opportunity for Patients, Regulators, Payors and Industry alike

      Presentation
    Michael Zaiac

    Michael Zaiac Head of Medical Affairs Oncology Region Europe
     Novartis

  • 10:30

  • Business Card Exchange with Morning Coffee/Tea & Discussion

     

         

  • 10:50

  • Implementing the right COAs, the right way, to support the patient experience in trials

    Anthony Mikulaschek

    Anthony Mikulaschek Vice President, eCOA
     IQVIA Technologies

    Elan Josielewski

    Elan Josielewski Senior Principal and head of Operations of Patient Centered Solutions
     IQVIA Technologies

  • 11:20

  • The complementary roles of RWE and trials to determine treatment effects

      Presentation
    Nawab Qizilbash

    Nawab Qizilbash Clinical Epidemiologist & Head of OXON
     OXON Epidemiology

  • 11:50

  • Noala Clinical Research Study Presentation

     

    The Noala DLD Program is effective in increasing receptive and expressive language skills in children aged 1-7 with delayed language skills

      Presentation
    Sarah Lyons

    Sarah Lyons Clinical Director
     Noala

Patient Recruitment & Site Selection

  • 12:15

  • Pioneering AI for community engagement, operations, and diversity in research

    • Digital transformation in patient/community engagement and recruitment.
    • Role of AI technology in engagement in DE&I.
    • Using data automation to scale operations and resourcing
      Presentation
    Amber Hill

    Amber Hill Founder and CEO
     Research Grid

  • 12:40

  • Luncheon & Networking - Visit Exhibitor Booths & Network with your peers in our Lounge

     

                

  • 13:20

  • Medical Affairs and Clinical Operations collaborating on Clinical Trial Optimization

    Viraj Rajadhyaksha

    Viraj Rajadhyaksha Area Medical Director
     AstraZeneca

  • 13:50

  • Innovative analytic technologies for predictive modelling, forecasting and optimal designing patient recruitment in clinical trials

    • Advanced technologies to maximize patient recruitment predictability at different stages
    • Optimal time-cost efficient recruitment design, sites/countries selection
    • Data-driven re-projection and optimal adjustment of recruitment
    • Centralized statistical monitoring and detecting unusual data patterns
    • Predicting event counts in event-driven trials
      Presentation
    Vladimir Anisimov

    Vladimir Anisimov Principal Data Scientist, Center for Design & Analysis
     Amgen

  • 14:20

  • How Can African Sites be routinely included? Addressing diversity at its core

    • Addressing and overcoming the fears
    • Understanding and removing the challenges
    • Providing robust tools to gather evidence
       
      Presentation
    Tina Barton

    Tina Barton Chief Operating Officer
     eMQT

    Shalom Lloyd

    Shalom Lloyd Co-Founder & Chief Strategy Officer
     eMQT

  • 14:50

  • Panel discussion: Critical Success Factors while Planning for Site Selection and Patient Recruitment

    • Discover sites with a demonstrated track record of good execution in trials
    • Study and site staff with solid certifications to expand the likelihood of powerful enrolment and an effective trial.
    • Factors such as disease prevalence rates, treatment practices, regulatory requirements and statistical considerations must be considered.
    • Access to subject population with the required eligibility criteria
    • Network within industries
    Nancy Meyerson-Hess

    Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
     eMQT

    Diane Driver

    Diane Driver Head Program Delivery
     UCB

    Carole Scrafton

    Carole Scrafton Patient & Health Advocate
     FibroFlutters

    Amelia Hursey

    Amelia Hursey Research Manager
     Parkinson's Europe

  • 15:20

  • Grab your Tea/Coffee - Visit our Exhibitor Booths & Network with your colleagues

     

         

Patient Centricity & Patient Engagement

  • 15:40

  • Play the long game: Plan for clinical trial success.

      Presentation
    Natalie Wilson

    Natalie Wilson Business Development Manager
     NIHR Clinical Research Network

  • 16:10

  • EU-PEARL: An EU patient-centric clinical trial platform

    Nadir Ammour

    Nadir Ammour Global Lead, Clinical Innovation & External Partnership
     Sanofi

  • 16:40

  • Patient partnering strategies in clinical research

    • How can current systems assist researchers assess which method of engagement could work best
    • How users can have an active role in setting your research priorities
    • Working in partnership with Patient organisations - shared learning and insights
      Presentation
    Amelia Hursey

    Amelia Hursey Research Manager
     Parkinson's Europe

  • 17:10

  • The importance of patient advocacy for clinical research.

      Presentation
    Carole Scrafton

    Carole Scrafton Patient & Health Advocate
     FibroFlutters

  • 17:40

  • Chairperson’s closing remarks

    Nancy Meyerson-Hess

    Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
     eMQT

  • 17:50

  • Networking Drinks Session


Thursday - 11th May 2023

  • 08:30

  • Registration & Refreshments

  • 08:50

  • Chairperson’s opening remarks

    Nancy Meyerson-Hess

    Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
     eMQT

  • 09:00

  • Remote Inspection and Audit

      Presentation
    Seif Eddine Amara Madi

    Seif Eddine Amara Madi Senior Manager Clinical Labs Quality
     GSK

  • 09:30

  • Empathy: a crucial ingredient to improve (diverse) patient recruitment and retention in clinical trials

      Presentation
    Roger Legtenberg

    Roger Legtenberg Senior Partner & Co-Owner
     Admedicum

  • 10:00

  • How Real-World Evidence and Real World Data Can Help Regulatory Agencies Make More Informed Decisions

      Presentation
    Andrew Gray

    Andrew Gray Global Regulatory and R&D Policy
     Amgen

  • 10:30

  • Business Card Exchange with Morning Coffee/Tea & Discussion

     

         

Clinical Data & Tech Driven Clinical Trials

  • 10:50

  • Interpretation and Impact of Real-World Clinical Data

      Presentation
    Mohamed Sharaf

    Mohamed Sharaf EMEA Senior Medical Advisor
     Janssen Europe, Middle East & Africa

  • 11:20

  • Standardisation and deployment of novel digital biomarkers in decentralised clinical trials and recent developments in AI (ChatGPT)

      Presentation
    Meelis Lootus

    Meelis Lootus Member of IEEE Novel Biomarkers for Decentralised Clinical Trials Working Group
     IEEE

  • 11:50

  • Interactive Response Technologies - Best Practices for Remote User Acceptance Testing.

    • IRT in a post-covid era
    • Modern challenges for UAT
    • Best practices for an efficient and successful Remote UAT
      Presentation
    Kate Chapman

    Kate Chapman Director
     Clinical Technology Consultants Ltd

  • 12:20

  • Strategies for globalization in clinical trials

    • Connecting the developed and the developing nations
    • Dealing with differences owing to culture and ethnicity
    • Role of CROs and third party stakeholders
    Francis Crawley

    Francis Crawley Executive Director
     Good Clinical Practice Alliance - Europe (GCPA)

  • 12:50

  • Luncheon & Networking - Visit Exhibitor Booths & Network with your peers in our Lounge

     

                

  • 13:30

  • RBQM: Align Monitoring Strategy to Quality Risk Assessment

    Shawntel Swannack

    Shawntel Swannack Director, Central Monitoring and Data Analytics
     GSK

  • 14:00

  • Global Clinical Development – Complex Generics

      Presentation
    Siddharth Chachad

    Siddharth Chachad Founder & Chief Strategist
     Reguclin Consulting

  • 14:30

  • From Insight to Action: Leveraging Enterprise Data for Strategic Decision-Making

      Presentation
    Jana Glogowski

    Jana Glogowski Insights Partner & Product Manager
     Roche

Outsourcing & Clinical Trials

  • 15:00

  • Feasibility in clinical trials

      Presentation
    Rali Vaskova

    Rali Vaskova Strategic Partnerships & Solutions
     FindMeCure

  • 15:30

  • Grab your Tea/Coffee - Visit our Exhibitor Booths & Network with your colleagues

     

         

  • 15:50

  • Panel Discussion – Partnering for progress - How Collaborative partnerships are transforming clinical trials?

    • Managing continuous & real-time collaboration
    • How transparency will lead to industrywide collaboration
    • Both sponsor and CRO must invest time in defining goals, anticipating issues and measuring results
    Nancy Meyerson-Hess

    Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
     eMQT

    Diane Driver

    Diane Driver Head Program Delivery
     UCB

    Kate Chapman

    Kate Chapman Director
     Clinical Technology Consultants Ltd

    Roger Legtenberg

    Roger Legtenberg Senior Partner & Co-Owner
     Admedicum

  • 16:20

  • Analysis of Real-World Data for clinical research and drug development

    • INC & EXC Criteria: Consensus resulted from a political game
    • INC & EXC Criteria: Universality and reproducibility in RWD?
    • RWD challenges for the ClinOps’s team:
    • From where the RWD datasets will come from?
    • Can they be audited?
    • How will it match the CT protocol IN & EXC?
      Presentation
    Aldir Medeiros Filho

    Aldir Medeiros Filho Former Senior Project Manager - Data Sciences Department
     Mitsubishi Tanabe Pharma Europe Ltd

  • 16:50

  • Chairperson’s closing remarks

    Nancy Meyerson-Hess

    Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
     eMQT

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Bring your team and get an extra discount. There are special group packages available. Please email to delegate@corvusglobalevents.comfor more details.

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For enquiries please e-mail to mediapartner@corvusglobalevents.com

VENUE

 

Holiday Inn London - Kensington
Wrights Lane, Kensington
London W8 5SP
United Kingdom

We make every effort to secure the very best hotel for our attendees with amazing event spaces, so that we’re able to guarantee our attendees the highest quality service and comfort.

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