3rd Operational Excellence in Clinical T

16-17 April 2025

3rd annual Operational Excellence in Clinical Trials Summit

WHO SHOULD ATTEND

CONFERENCE BENEFITS

''Even though a study may be very well designed and funded, it cannot bring a drug to market without the availability of suitable subject.“

OECT Summit in New Jersey, USA is targeted for professionals who are always seeking for new opportunities, visionary ways of conducting performance. Study Feasibility, Site Management, Monitoring and Patient recruitment & Patient Retention offer major challenges to the executives from clinical researcher, clinical project, clinical operations, innovation, intelligence, medical Operations with potential for significant impact on time lines, budgets, CRA talent rejuvenation, collaborations & partnerships and ultimately the scientific integrity of the trial itself.Many factors affect the recruitment of patients and difficulty in finding suitable patients is driving the development of many innovative methods for accessing new patient groups. How the Risk Based Monitoring and Big Data can have a significant impact in clinical trials.The artificial intelligence, innovative channels of communication, rise of social media & Blockchain means that new technologies and changing strategies for communication can be used to have feasibility right at first & great effect to reach out to patients directly.Additionally outreach through patient advocacy groups/communities, social service agencies are becoming more important to communicate with patients viable for trial participation as well as for those already enrolled in clinical trials. How to maximise the benefit of this approach and ensure our regulatory obligations are appropriately met will be the subject of several sessions during the summit.

Click here for the Two days Agenda Schedule

You should not miss this annual opportunity if you are - Chiefs, Directors, Heads, Senior Manager, Leaders and Executives from:

Clinical Operations
Clinical Developments/Research/Innovation
Clinical Intelligence
Clinical Program
Clinical Project Management
Study Feasibility
Site Management
Study Monitoring Operations
International Clinical Research
Patient Recruitment & Retention
Medical Operations
Medical Affairs/Advisors
MSL
Data Management
Compliance and Regulatory
Patient Advocacy

For group discounts and complete details contact us.

REQUEST FULL AGENDA

OVERVIEW

Opportunity to meet top expert and decision makers from Pharma, Biotech, Medical Devices, Clinical Sites and CROs industry under one Roof

Get engaged with the professionals from leading industries
20+ Keynote Sessions
5+ Workshop sessions
Round Table Discussions – Brain storming
Panel Discussions – Interact Directly with the Panellists to raise your challenges
More than 10 Case Studies presenting by the top experts from across the industry
13+ hours Networking Opportunity
Benchmarking Opportunities
One-to-one interactions
Tea/Coffee Breaks, Social Events and Cocktail Reception
.…and much more!

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About KP-Morgan Group

KP Morgan specializes in clinical trials, SFE, commercial excellence and Healthcare innovation events, hosting events in various locations such as Canada, USA, Europe and Dubai.

KP-Morgan Conferences have provided platforms for debate across many industry sectors including: Telecommunication, banking & financial services, retail and FMCG, investments, pharmaceuticals, IT, chemical & petro chemical.

Many argue that the innovation process cannot be managed because innovation is supposed to be about creativity and cannot be predicted. We believe in KP-Morgan that Innovation is not only about being creative and inventive; innovation is a collaborative process where ideas are taken and managed through to value-adding market introduction.

The consistent high quality of our events has given rise to a reputation for excellence, ensuring that KP-Morgan conferences provide the most fertile ground for participants to gain up-to-the-minute market intelligence and invaluable opportunities to network and generate new business.

INTERESTED IN EVENT PARTNERSHIP?

AGENDA: TOPICS AT GLANCE

Keynote Presentation, Interactive Discussions, Case Studies, Brain Storming and Round Table Discussions

OPEX, Study Feasibility and Site Selection, Activation, Management

Beyond Monitoring your Clinical Trial: Best Practices in Applying RBQM
Future Trends in Study Feasibility and Site Management
Complex Regulatory Environment: Diversified Market Challenges
Hurdles of Data Management and Integration
How to gain actionable insights and improve decision-making processes?
Investigator Motivation in Clinical Trials and how it affects enrolment in studies
Complex of SOPs & eConsent
Changing Roles of Clinical Project Leaders
Communication barriers in CROs, Sponsors & Sites: Key to successful partnership
Let's Make it work: Time, Quality, Budget & Rare Disease!
Leadership, Coaching and Motivating
Managing Site Performance and how to motivate site staff?
Voice of Patient in study design and start-up
Future of Data Driven Clinical trials
Sponsor & CRO impact on enrollment of sites
Use the TMF as a strategic study asset

How data and technology platforms accelerating the feasibility process?
PI engagement: Role of sites
Solution to unmet clinical trial needs: Investigators perspective
Design Tools to effectively plan, manage and track your clinical study portfolio
How to optimize digital tools to accelerate operations?
How to optimizing resource allocation to maximize ROI?
Evolution of data science in data management
Data driven decision making
Leveraging RWD for Clinical Research
Vendor Oversight & relationship in Clinical operations
Data Management: Integrating diverse data sources efficiently in quality and time manner
Digital vs Human Behaviour: CRA of the Future
Engaging Sites and investigators: Optimizing Study Design
How to improve site relationship
Importance of Embracing Change to Optimize Clinical Research
Navigating Global Challenges with Innovative Approaches
Importance of Patient-Centric Trial Design

PATIENT EMPOWERMENT: AS PARTER

Enrolment Planning and Patient Recruitment
Role of communities & advocacy groups in planning & patient recruitment
Rethinking the path to enrolment: Planning and Recruitment
Holistic approach to patient recruitment: Case Study
Data Driven Approaches to Enhancing Retention
Optimize Patient Outcomes and Promote Health Equity
Patient Engagement: Diversity, equity & inclusion
How the needs of patients have evolved clinical trials
Re-defining Patient Value Transformation
Patient Experience & Compliance: opposing forces?
Drivers and Barriers for Patient Engagement
Touch Points in a Patient’s Journey
How Pharma Companies Can Partner with Patients for Better Patient Experience?
Data Science as key pillars to patient recruitment

Demonstrating Patient Insights at early drug development
Understanding technology advancement at patient level
What is the future of innovative medicines development?
Despite digital acceleration, how to remain Patient centric
Bridging the two worlds, Clinical and Medical: key to enabling stakeholders at all levels
The challenging path to patient centricity: breaking down silos to achieve the ultimate goal
Trends in Medical Devices industry: Driving growth
The Role of Technology(mobile apps etc) in Enhancing Patient Retention
Retention Strategies in Long-Run Clinical Trials
Patient Retention: Who own the Future of Next Generation Clinical Trial Innovation?
Using patient insights for feasibility excellence
Cross Functional KPIs
Diversity & Inclusion