Workshop title: Introduction to Clinical Trials for Healthcare Professionals
Module 2: Roles and responsibilities of investigators, nurses, and allied health professionals.
The second of five modules. This module focuses on CRA Responsibilities, Documentation, and Record-Keeping.
Speaker: Mr. Olumide “Olu” Olufuwa, MBBS, FWACS, FMCR
Olumide Olufuwa (“Olu”) is a Senior Clinical Research Associate at a cell therapy biotechnology company developing curative treatments for solid malignant tumours. With a background in Microbiology, Nursing, and an MSc in Bioinformatics, Olu combines bedside and bench-side expertise to support global clinical operations. His experience as a bone marrow transplant and research nurse enhances his ability to train stakeholders and foster collaborations with research sites, regulators, and vendors. A former university lecturer in Finland, Olu also mentors life science professionals transitioning into clinical research roles and is an active speaker and advocate for diversity in clinical trials.
Speaker: Angela Agore, Registered Nurse/Clinical Research
Angela Agore, MRes, RGN, BSc, is the Lead Research Nurse at an NHS Trust in the UK, leading research initiatives across Southeast London and Kent, including the Galleri early cancer detection trial. She holds a BSc in Nursing from the University of Ghana and an MRes in Clinical Research from King’s College London. With over a decade of experience in Ghana and the UK, Angela champions inclusivity and BAME participation in research. As PPIE lead, she established the Public Research Champions program and co-directs research for the Ghanaian Diaspora Nursing Alliance.
Objectives:
By the end of this workshop, participants will be able to:
- Describe the key phases, design types, and operational components of clinical trials within global and African health contexts.
- Gain knowledge on the core principles of ICH-Good Clinical Practice to ensure ethical and compliant participation in clinical research.
- Identify the roles and responsibilities of nurses, physicians, and allied health professionals in patient recruitment, informed consent, and trial conduct.
- Demonstrate understanding of data integrity, participant safety, and community engagement strategies that support high-quality trial outcomes.
- Evaluate opportunities to integrate clinical research practices within their professional settings
Date: Thursday, 27th of November 2025
Time: 1 PM EST / 6 PM GMT
Duration: 90 minutes