Conference Overview

The Global Clinical Trials Connect 2022 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.

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 2022.

 


Conference Streams Include

 

 

Globalisation in Clinical Trials

Optimizing Trial Design

Patient Recruitment & Retention

Site Selection & Feasibility

Patient Engagement & Patient Experience

Partnerships & Outsourcing

Clinical Trial Budgets and Contracts

Quality & Compliance

Risk based Trial Management

Clinical
Operations

Clinical Trial Regulation

Data
Management

Tech-Driven Clinical Trials

Decentralized Clinical Trials

Future Clinical
Trials

 

 

 

KEY DISCUSSIONS WE'LL BE EXPLORING

  • 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
  • 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

VIEW ALL

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

For enquiries on speaker opportunities please e-mail to [email protected]



Wednesday - 21st September 2022 (Time Zone - BST) - Virtual Conference

  • 09:30
  • Welcome Address & Platform Orientation - Orientation will focus on how to access and navigate the virtual conference platform for Live Sessions & Interactive Networking

  • 09:40
  • Chairperson’s opening remarks


    Nancy Meyerson-Hess

    Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
    eMQT

  • 09:50
  • Transforming the Way We Do Clinical Trials: Pragmatic Trials Combined with EHR Enabled Services


    Mats Sundgren

    Mats Sundgren Director Health Informatics
    AstraZeneca

  • 10:15
  • Novel approaches in Clinical Trial Design to Improve Efficiency of Research

    • Strategies & Methods for flexible design trials
    • The Adoption and Impact of Adaptive Trial Designs
    • Preclinical environment and trial designs Opportunities and Limitations

     

    For sponsorship opportunities please contact: [email protected] or call +44 (0) 207 096 0786

  • 10:40
  • Learnings from a Fully Decentralized Trial in Oncology and a Hybrid Decentralized in Autism

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

    Thomas Wiese

    Thomas Wiese Principal Medical Director, Clinical Expert Team Leader
    Roche

  • 11:05
  • How the World Health Organization’s International Clinical Trials Registry Platform (ICTRP) is improving research transparency globally.


    Ghassan Karam

    Ghassan Karam Project Manager
    World Health Organization

Patient Recruitment & Site Selection

  • 11:30
  • How Digital recruitment is changing the face of clinical trials


    Livia Dixon

    Livia Dixon Director Digital Recruitment Strategist
    Novartis

  • 11:55
  • Advanced analytic technologies for predictive modelling and optimizing patient recruitment in clinical trials

    • Analytic modelling and forecasting patient recruitment
    • Optimal operational design, sites/countries selection given costs & time constraints
    • Data-driven re-projection and optimal adjustment of recruitment to increase probability to meet target
    • Centralized statistical monitoring and detecting unusual data patterns
    • Predicting some operational characteristics

    Vladimir Anisimov

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

  • 12:20
  • Virtual Luncheon & Networking - Visit Exhibitor Booths & Network with your peers in our Lounge (Face to Face Video Chats)

     

                

  • 13:00
  • True Global Diversity in our Trials: Africa is Ready


    Shalom Lloyd

    Shalom Lloyd Co-Founder & Chief Strategy Officer
    eMQT

    Tina Barton

    Tina Barton Chief Operating Officer
    eMQT

  • 13:25
  • Feasibility in clinical trials - the main ingredients

    • Importance of conducting feasibility
    • The stages of clinical trial feasibility
    • Feasibility challenges

    Dex Bilkic

    Dex Bilkic Senior Manager, Site Engagement
    Bayer

  • 13:50
  • Consent Transformation: a Requirement for Digitization of Trials


    Brenda Yanak

    Brenda Yanak Advisor

  • 14:15
  • Panel discussion: Effective patient recruitment and retention in clinical trials to boost trial success

    • What will persuade and impact the patient?
    • Is there anything pharma can provide for a trial member that will increase the value of participation?
    • The aim of patient-driven clinical trials is to diminish the burden of participation by making the participant journey as convenient and pleasant as possible
    • Utilize fitting procedures and techniques to limit dropouts without, in any capacity, constraining a patient to remain in the study

    Lauren Bataille

    Lauren Bataille Head, Digital Medical Capabilities
    Novartis

    Carole Scrafton

    Carole Scrafton Patient & Health Advocate
    FibroFlutters

    Vladimir Anisimov

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

    Nancy Meyerson-Hess

    Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
    eMQT

  • 14:40
  • Global Clinical Development – Complex Generics


    Siddharth Chachad

    Siddharth Chachad Executive Vice President & Head - Global Clinical Management
    Dr. Reddy's Laboratories

Patient Centricity & Patient Engagement

  • 15:05
  • Bringing the patient voice in the design of clinical trials and how patient engagement/inclusiveness must be planned and implemented throughout the lifecycle of clinical development


    Lea Proulx

    Lea Proulx Patient Voice Partner
    Roche

  • 15:30
  • Visit Virtual Exhibitor Booths/Speed Networking at our Exclusive Lounge (Face to Face Video chat with Exhibitors and other attendees)

     

         

  • 15:50
  • Integrating the Patient Voice into Medical Product Development: Opportunities and Applications for the Use of Patient Experience Data


    Jessica Abel

    Jessica Abel Director, Patient Experience Data Policy and Best Practices
    Abbvie

  • 16:15
  • What are the benefits of using multi stakeholder approaches, in research, from the patient perspective

    • Why are multi-stakeholder approaches needed and important?

    • Leveraging collaboration to address patients' needs and challenges

    • The impact of multi-stakeholder approaches on reducing patient burden

    • Patient experience and perspective taking part in multi-stakeholder initiatives


    Carole Scrafton

    Carole Scrafton Patient & Health Advocate
    FibroFlutters

  • 16:40
  • Patient Engagement in Clinical Development - A look at what the UK are doing to bring patients to the forefront of study design


    Alex Hammond

    Alex Hammond Business Development Manager
    NIHR Clinical Research Network

    Kim Down

    Kim Down Business Development Manager
    National Institute of Health and Care Research (NIHR)

  • 17:05
  • The Integration of Patient-Centricity Across the Lifecycle of Treatment Development


    This talk provides a broad view of the rapidly developing landscape of Patient-Centricity in Clinical Research. The audience will learn about a variety of initiatives aimed at improving and accelerating clinical research through collaboration with patients, advocates and their communities.

    • Explore research measuring and evaluating the "Return on Engagement" financial and efficiency value of Patient Centric activities
    • Review key regulatory developments in support of Patient Centered Research
    • Gain insights from the largest global survey on patient and public perceptions and experience in clinical research
    • Examine concrete examples of Patient Centered Research programs and project

    Behtash Bahador

    Behtash Bahador Director, Health Literacy
    CISCRP

  • 17:30
  • Panel discussion: The patient's perspective: why their voice is so important in clinical research


    Jost Leemhuis

    Jost Leemhuis Safety Science Partner and Global Business Lead
    Roche

    Nancy Meyerson-Hess

    Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
    eMQT

    Mary Lynne Van Poelgeest-Pomfret

    Mary Lynne Van Poelgeest-Pomfret International patient advocate
    World Federation for Incontinent Patients - WFIP

  • 17:55
  • Interactive Breakout Discussions:

     

    All the participants will have a great opportunity to discuss and explore a selection of most interesting topics discussed during the conference in small groups with their industry colleagues in an informal setting.

     

    Round Table 1: Innovation in Clinical Trials - Digital Approaches

     

    Round Table 2: Patient Centricity

     

    Round Table 3: Globalization and Country Specifics

     

    Round Table 4: Recruitment Challenges - Patients and Sites

     

    Round Table 5: Changing Clinical Trials - What needs to be addressed

     

    Round Table 6: Patient Retention

  • 18:20
  • Chairperson’s closing remarks


    Nancy Meyerson-Hess

    Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
    eMQT

  • 18:30
  • Networking - Catch-up with your peers in social lounge


Thursday - 22nd September 2022 (Time Zone - BST) - Virtual Conference

  • 09:30
  • Welcome Address & Platform Orientation - Orientation will focus on how to access and navigate the virtual conference platform for Live Sessions & Interactive Networking

  • 09:40
  • Chairperson’s opening remarks


    Nancy Meyerson-Hess

    Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
    eMQT

  • 09:50
  • Deploying a DCT in Europe – learnings from the IMI [email protected] Initiative


    Rebecca Jackson

    Rebecca Jackson Sr. Mgr. Clinical R&D Innovation & Novel Modalities IT
    Janssen Pharmaceutical

  • 10:15
  • Enrolment and retention in clinical studies before and during Covid-19 pandemic: clinical challenges and new opportunities. A case report from a phase 3 clinical program in fibromyalgia


    Domenico Merante

    Domenico Merante Global Clinical Development TA Lead Nephrology and Orphan Disease Area
    Vifor Pharma

Decentralized Clinical Trials

  • 10:40
  • Patient centric trials to increase Diversity and generate more patient care relevant outcomes from RCTs


    Michael Zaiac

    Michael Zaiac Head of Medical Affairs Oncology Region Europe
    Novartis

  • 11:05
  • Optimizing your Decentralized Clinical Trials with Real-World Data

     

    For sponsorship opportunities please contact: [email protected] or call +44 (0) 207 096 0786

  • 11:30
  • Setting up Your Decentralised Trial for Success

    • New business model based on the Technological advances and research activities integrated seamlessly into clinical trials
    • Developing custom made contracts by third-party vendors, CROs and sponsors for modern clinical trials

    Angel Soubhie

    Angel Soubhie Head clinical trial scientists - Medical Director
    Bayer

Outsourcing & Clinical Trials

  • 11:55
  • A key factor in vendor Selection - The role of the CRO in advancing patientcentric clinical trial approaches


    Jan Schmejkal

    Jan Schmejkal Associate Director, Global Trial Leader
    The Janssen Pharmaceutical Companies of Johnson & Johnson

  • 12:20
  • Virtual Luncheon & Networking - Visit Exhibitor Booths & Network with your peers in our Lounge (Face to Face Video Chats)

     

                

  • 13:00
  • Panel Discussion - A collaborative clinical ecosystem: How to effectively manage partnerships with all Stakeholders including Patients, Sites, CROs, Sponsors and Regulators.


    Nancy Meyerson-Hess

    Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
    eMQT

    Sonia Houston Pichardo

    Sonia Houston Pichardo Business Lead of MyStudyWindow
    Boehringer Ingelheim

Quality, Compliance & Risk Management

  • 13:30
  • The effectiveness of new generation analytics models in RBM

    • Centralized monitoring can characterize key risk classifications and pointers from all clinical and operational source data available.
    • To evaluate risks to site performance, subject safety and data quality using Data and Analytics
    • Differentiating the relative risks between sites and subjects using the new age analytics models.

    Shawntel Swannack

    Shawntel Swannack Director, Central Monitoring and Data Analytics
    GSK

  • 13:55
  • Navigating and applying risk based approaches in clinical trials


    Laura Galuchie

    Laura Galuchie Senior Director & TransCelerate Program Lead
    MSD

  • 14:20
  • Are we obsessed with Quality Tolerance Limits?

    • Choosing QTL Parameters wisely
    • Are you asking the right questions when considering the application of Quality Tolerance Limits (QTL)?
    • Controlling risk within diagnostic clinical studies

    Mireille (Zerola) Lovejoy

    Mireille (Zerola) Lovejoy Director of Clinical Risk Management
    GE Healthcare

Clinical Data & Tech Driven Clinical Trials

  • 14:55
  • FDA draft guidance on 'Digital Health Technologies for Remote Data Acquisition in Clinical Investigations


    Benoit Marchal

    Benoit Marchal Chief Digital Trust Officer
    Partners for Patients

  • 15:20
  • Visit Virtual Exhibitor Booths/Speed Networking at our Exclusive Lounge (Face to Face Video chat with Exhibitors and other attendees)

     

         

  • 15:40
  • Evidence derived from RWD through the application of research methods


    Mohamed Sharaf

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

  • 16:05
  • Making Decentralizing Clinical Trials Pragmatic with AI and Wearables


    Maria Palombini

    Maria Palombini Leader, Healthcare Life Sciences Practice
    IEEE Standards Association

  • 16:30
  • Leverage AI to create value in Clinical Trials

  • 16:55
  • Panel Discussion: The Future of Clinical Trials - The Role of Advanced Analytics and Artificial Intelligence


    Jessica Riggleman

    Jessica Riggleman Sr. Director, Clinical and Regulatory Affairs
    Mydecine Innovations Group

    Mohamed Sharaf

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

    Bhupathy Alagiriswamy

    Bhupathy Alagiriswamy Director
    Credence Clinical Solutions Ltd

    Nancy Meyerson-Hess

    Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
    eMQT

  • 17:25
  • Novel techniques- Tech-driven clinical trials

    • Effectively using Technology is enabling patient centricity
    • How to implement mobile technology and make it work in clinical trials
    • Does consumer technology devices used in clinical trials?
    • IoT in digital transformation of clinical trials

     

    Speaker TBC - Slot booked for Gavion Technolgoies

  • 17:50
  • Decentralized Clinical Trials and Patient Centricity: Spotlight on Rare Diseases

    • Uses & challenges for Blockchain in Clinical Trials
    • Storing all types of data safely and securely
    • Better Clinical Trials Quality

    Oscar Segurado

    Oscar Segurado Chief Medical Officer
    ASC Therapeutics

  • 18:15
  • Chairperson’s closing remarks


    Nancy Meyerson-Hess

    Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
    eMQT

What do the Pass Include


  •  C-Suite keynote sessions & Panel Discussions
  •  Full 2-day live event Access
  •  Interactive live Video chat
  •  Interactive Social lounge with individual tables for discussions & Exchange of Information
  •  Q&A Session and polling
  •  Messaging meetings and networking with Industry Experts and Peers
  •  Access to Virtual expo (including videos, reports and articles from solution providers),
  •  Receiving Handouts
  •  On demand event recordings until 1 month
  •  Certificate for attending

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