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

DUBLIN–(BUSINESS WIRE)–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 medical trials and medical analysis.

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

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

This convention intends to deal with the worldwide well being and medical trials around the globe. Bioethics, rules, affected person recruitment, website choice, actual-world information, information integration & Strategy, outsourcing, vendor administration, high quality (QbD) in Trial Conduct, threat-primarily based monitoring, medical auditing & monetary planning and different important matters that play a key function in medical trials will likely be addressed together with revolutionary 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 features, report on medical trials and achieve a greater data of the implications of medical trials in prevention, prognosis, medical trial-associated ethics and illness remedies.

The Virtual summit will facilitate a useful networking alternatives with Decision makers and Industry consultants, specializing in actual case research and insightful shows. Bringing in Exciting options like Q&A Sessions with business consultants, 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 broaden 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 medical trials
  • Making Patient Engagement a Reality
  • New improvements in Patient Recruitment planning and execution on a medical trial
  • Outsourcing methods and fashions
  • Electronic Clinical Outcome Assessment and Electronic Patient Reported Outcome
  • Streamlined IRT growth course of
  • Pharmacovigilance & Clinical Trials
  • Post-Clinical Trial closed communities
  • How to future proof your medical operations
  • Implementing Risk Based Monitoring
  • Streamlining R&D and decrease prices in medical 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 expertise for bettering medical analysis high quality

Who Should Attend:

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

Attendees embody 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 marketing consultant

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


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

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