Two Day Virtual Clinical Trials Connect Conference 2021: Futuristic Advancements in Clinical Trials and Clinical Research – May 5th-6th, 2021 – | Business


The “Global Clinical Trials Connect 2021” convention has been added to‘s providing.

The 4th Annual Global Clinical Trials Connect 2021 will present a platform to debate on the futuristic developments in scientific trials and scientific analysis.

This multidisciplinary program includes broad participation of individuals from scientific trials neighborhood from across the globe who’re targeted on studying extra about scientific analysis, scientific trials planning and administration.

The Pharma and Bio-Tech corporations are constantly evolving and new scientific research, applied sciences and developments in care and remedies have augmented the effectivity and on the similar time, the complexity of scientific trials has elevated, with checks being carried out in a extremely structured and intently coordinated method. It is excessive time that we glance into progressive methods, new applied sciences, efficient and high quality collaborations to handle these points, which may cater to the wants of the affected person and the business.

This convention intends to deal with the worldwide well being and scientific trials world wide. Bioethics, laws, affected person recruitment, web site choice, actual-world information, information integration & Strategy, outsourcing, vendor administration, high quality (QbD) in Trial Conduct, danger-based mostly monitoring, scientific auditing & monetary planning and different important matters that play a key function in scientific trials will probably be addressed together with progressive classes on new applied sciences, efficient and high quality collaborations.

This program will definitely educate well being care scientists on trial design, operations, organizing trials, analysis computing, regulatory facets, report on scientific trials and acquire a greater information of the implications of scientific trials in prevention, prognosis, scientific trial-associated ethics and illness remedies.

The Virtual summit will facilitate a useful networking alternatives with Decision makers and Industry specialists, specializing in actual case research and insightful displays. Bringing in Exciting options like Q&A Sessions with business specialists, Networking Video Chat, Polling, Raise Hand, Virtual Exhibitor cubicles with ready room/tables and digital chat, Peer to Peer join at Social Lounge, Handout Bags and extra giving alternative to develop and develop your networking all through the occasion

Key Highlights

  • Patient Recruitment and Site choice
  • Innovative trial designs
  • Partnership & Collaboration – Sponsors, CROs, Sites and External Vendors
  • Patient centric scientific trials
  • Making Patient Engagement a Reality
  • New improvements in Patient Recruitment planning and execution on a scientific trial
  • Outsourcing methods and fashions
  • Electronic Clinical Outcome Assessment and Electronic Patient Reported Outcome
  • Streamlined IRT improvement course of
  • Pharmacovigilance & Clinical Trials
  • Post-Clinical Trial closed communities
  • How to future proof your scientific operations
  • Implementing Risk Based Monitoring
  • Streamlining R&D and decrease prices in scientific trials
  • Adaptive Trial Model
  • Clinical Trial Auditing
  • Real World Clinical Trial Strategies
  • Data Quality & Technology
  • Clinical Data Strategy & Analytics
  • Electronic Data Capture (EDC) Systems
  • Clinical Technology and Driving Innovation
  • M-Health, Wearable and Consumer Technology
  • Big-Data, IoT and Artificial Intelligence in Clinical trials
  • Blockchain know-how for bettering scientific analysis high quality

Who Should Attend:

This occasion is designed for senior-degree attendees from varied corporations together with Pharmaceutical, Bio-Tech, Bio-Pharma, CRO’s, Investigative Sites, Solution supplier and Government establishments.

Attendees embrace 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
  • IT
  • Clinical Data Management
  • EDC
  • Clinical/Digital Innovation
  • Clinical Design/Protocol design/ Strategy makers
  • Clinical Research Sites
  • CROs and CMOs
  • Hospitals/ Associations
  • Regulatory affairs


Daniel De Schryver

Patient Engagement & Advocacy Lead, EMEA

Janssen Pharmaceutical

Catherine O’Connor

Director, Global Clinical Research

Gilead Sciences

Adama Ibrahim

Director, Digital Solutions (Global Drug Development)


Bodo Lutz

Global Risk Management, Data Integrity, and Quality Assurance


Ana Herradon Virseda

Associate Director, Monitoring Manager

Bristol-Myers Squibb

Maria Kuthning

Clinical Program Leader

Sobi – Swedish Orphan Biovitrum AB (publ)

Pawel Wojcik

Associate Director Study Management (Clinical Operations, R&D Oncology)


Maria Palombini

Leader, Healthcare Life Sciences Practice

IEEE Standards Association

Tamzin Blagbrough

Sourcing guide

Eli Lilly

Sol Yates

Associate Director Regulatory Affairs Development


Veronique Freund

Head of Clinical External Parties Quality Management


Edyta Zbirog-Lukawska

Central Europe Quality And Compliance Adviser (Affiliate Process and Training Adviser)


Lucy Hampshire

Senior Director, Medicines Quality

Eli Lilly and Company

Karen Hue

Senior GxP Consultant


Devaki Nair

Clinical Lead for Clinical Biochemistry and HOD – Director SAS Centre for Cardiac Biomarkers


Ellen Van Vijnckt

Head Start-Up & Admin Team Country Clinical Operations


Vladimir Anisimov

Principal Data Scientist | Data Science | Center for Design & Analysis


Nancy Meyerson-Hess

Chief Compliance and Regulatory Officer


Kylie Gyertson

Head of Cancer Clinical Trials Unit


Tim Cave

SaySo Medical CEO & Founder

SaySo Medical

Marc Ditmarsch

VP Clinical & Operations

NewAmsterdam Pharma

Gareth Powell

Business Development Officer


For extra details about this convention go to

View supply model on


Laura Wood, Senior Press Manager

[email protected]

For E.S.T Office Hours Call 1-917-300-0470

For U.S./CAN Toll Free Call 1-800-526-8630

For GMT Office Hours Call +353-1-416-8900



SOURCE: Research and Markets

Copyright Business Wire 2021.

PUB: 04/12/2021 10:35 AM/DISC: 04/12/2021 10:35 AM

Related Posts