2025년 컨퍼런스전 워크샵
2025년 2월 3일(월요일)
PRE-CONFERENCE WORKSHOPS: IN-PERSON ONLY
products. Join the journey.

1:00 - 1:45 pm WORKSHOP 2: Join and Explore ClinEco, SCOPE's B2B Clinical Trial Community and Marketplace 
Join this hands-on session with ClinEco, SCOPE’s B2B clinical trial community and marketplace featuring 850+ companies. ClinEco unites sponsors, CROs, service providers, and sites to streamline partnering, vendor research, innovation, and learning. At SCOPE 2024 we introduced the ClinEco Commons, a collaborative space where you can access, visit, and share valuable content as well as contribute to the wealth of knowledge within the SCOPE and ClinEco Community. This year we launch our 'Ask a ClinEco Luminary' program where members can connect directly, and discreetly, with industry leaders and receive insights on a wide range of clinical trial topics. Join now at: clineco.io/register. Open to all SCOPE attendees.
1:00 - 2:30 pm WORKSHOP 3: The Path towards Sustainable Clinical Trials: Reducing the Environmental Impact of Global Clinical Trials 
INSTRUCTORS:
 
Michael J. Cohen, Senior Director, Lead, Environmental Sustainability, PPD/Thermo Fisher Scientific
Thierry Escudier, Portfolio Lead, Pistoia Alliance
Hannah Sieber, Co-Founder, CEO, Artyc
Diana Steinbuesch, BioX Operations Portfolio Lead (Oncology), Roche
While developing leading and innovative therapies, we must not lose sight of the environmental impacts and greenhouse gas emissions. We can reduce the environmental impact of our studies by prioritizing remote visits and monitoring, by reducing kit wastage, and working together to find ‘greener’ solutions. This workshop will provide a brief overview of research and introductory strategies for reducing emissions as well as a 'Sustainability 101' to help anyone in our industry get started towards developing more environmentally responsible clinical trials. Open to all SCOPE attendees. Sustainable Healthcare Coalition is a Partnering Organization at SCOPE.
1:00 - 2:30 pm WORKSHOP 4: Efficient Importation of Biological Materials into the U.S.
INSTRUCTORS:
Jessica Hammes, Branch Chief, Biological Threat Exclusion, Agriculture Safeguarding and Risk Management, Agriculture Programs and Trade Liaison, Office of Field Operations, U.S. Customs and Border Protection
Jennifer Merriman, Senior Manager, Strategic Biospecimen & Vendor Logistics, Consent, Biospecimens, & Imaging, Global Development Operations, Bristol Myers Squibb Co.
(Additional speakers to be announced.)
U.S. Customs and Border Protection and partner government agencies regulate the importation of biological materials into the United States. The efficient importation of these items can be challenging, as Clinical Trial landscape is ever-evolving. The purpose of this workshop is to discuss current challenges, best practices, and possible solutions to navigate this landscape.
2:00 - 3:30 pm WORKSHOP 5: Sponsor and Site Perspectives: Addressing Current Challenges and Exploring Future Opportunities in Clinical Trial Financing
INSTRUCTORS:
Dawn Anderson, Partner, Consulting, Deloitte LLP
Ming Shen, Managing Director, Deloitte Consulting LLP
This workshop will explore sponsor and site perspectives on current challenges and future opportunities in clinical trial financing. It will address complexities in
    managing trial finance including estimation, budgeting, forecasting, invoicing, payments, reconciliation, and others in clinical trial management. The workshop aims to identify innovative solutions to enhance finance management in clinical trials, fostering more accurate projections. Through discussions and interactive sessions, it seeks to provide insights for future opportunities to improve clinical trial finance.
* 주최측 사정에 따라 사전 예고없이 프로그램이 변경될 수 있습니다.
2025월 프로그램
◆ Sunday Golf, Kick-Off Keynote &    Participant Engagement Award
월요일의 골프、킥오프 기조 강연、참가자 참여상
    
  
◆SCOPE’s Kickoff Reception
SCOPE의 킥오프 리셉션
◆ Patient Voice in Trial Design and Protocol Development
시험 디자인과 프로토콜 개발에서 환자의 소리
	
  
◆ Developing and Executing Effective Diversity Plans
효과적 다양성 플랜의 책정과 시행
	
  
◆ Enrollment Planning and Patient Recruitment
등록 계획·피험자 모집
	
  
◆ Patient Engagement and Retention through Communities and Technology
커뮤니티·기술에 의한 피험자 관여와 고객 유지
	
  
◆ Clinical Trial Forecasting, Budgeting and Contracting
임상시험 예측·예산 편성·계약
	
  
◆ Resource Management and Capacity Planning for Clinical Trials
임상시험의 리소스 관리·커패시티 플래닝
	
  
◆ Mastering an Outsourcing Strategy
아웃소싱 전략의 마스터
	
  
◆ Relationship and Alliance Management in Outsourced Clinical Trials
임상시험 아웃소싱에서 관계와 제휴 관리
	
  
◆ Digital Biomarkers and Endpoints in Clinical Trials
임상시험에서의 디지털 바이오마커와 엔드포인트
	
  
◆ Digital Measurements Implementation at Scale
대규모 디지털 측정의 실장
	
  
◆ Modernizing Lab, Biomarker & Data Management Operations
랩·바이오마커·데이터 관리 업무의 현대화
	
  
◆ Biomarker & Biospecimen Technology & Innovation
바이오마커·바이오 시료 기술과 혁신
	
  
◆ Data Technology for End-to-End Clinical Supply Management
E2E 임상 서플라이 관리용 데이터 기술
	
  
◆ Clinical Supply Chain Strategies to Align Process, Products and Patients
임상 공급망 전략으로 프로세스·제품·피험자를 연계
	
  










