Our Management Team
Musaiwale Kamfose, Co-Founder and Director
Musaiwale Kamfose is an Oxford graduate (Kellogg College) in Evidence-Based Medicine, a Harvard University Global Clinical Scholars Research Training fellow, and holds an MSc in Clinical Governance from the University of Dundee. He also has a BSc, a Diploma in Management, and a Doctorate in Health from Bath/Oxon Universities.
As a clinical researcher, Musaiwale has collaborated with various stakeholders in the health sector. He is passionate about advancing scientific understanding, improving clinical practice, and working with diverse teams and partners in research management.
Timothy Lubinda, MSc, Co-Founder
Timothy Lubinda is a seasoned clinical research operations professional with over 20 years of experience across multiple research sectors. His career spans roles in banking, NHS clinical trials site management, and university-based clinical research, including his tenure at Oxford University, where he served as a Programme Manager for the Oxford-AstraZeneca vaccine trials.
He has also held different roles in global and local clinical trials operations management in Pharmaceutical organizations. Timothy holds a BSc. Mathematics and Statistics and an MSc. Health Economics and Health Policy. He is also member of the association of clinical research professionals (ACRP) .
Bringing the Gap Between Clinical Practice and Research
Oxford Clinica was established in 2025 by a team of professionals with extensive experience in the health sector. Our mission is to address the critical gap between clinical practice and research by providing expert research management services.
Our Commitment
At Oxford Clinica, we are dedicated to supporting healthcare professionals and organisations in overcoming these challenges. By delivering tailored research solutions, we help ensure studies are conducted efficiently, safely, and within regulatory frameworks.
Expertise in Regulatory Compliance
International Regulatory Knowledge
We operate in strict accordance with global regulatory guidelines, ensuring compliance with key regulatory bodies such as the MHRA (UK), FDA (U.S.), EMA (European Union), TGA (Australia), and others. This enables us to conduct trials across multiple jurisdictions while upholding ethical and legal standards.
Local Expertise in Diverse Markets
Oxford Clinica understands the complexities of local regulations and tailors its processes to meet the specific needs of different regions. Our expertise ensures smooth and efficient trial operations worldwide.
Tailored Clinical Research Solutions
Flexible Study Designs
We offer tailored solutions for clinical trials, including Phase I-IV studies, observational research, and registry studies. Our adaptable approach ensures that each trial meets the unique needs of our clients, whether locally or globally.
Customizable Services for Any Region
Our ability to offer customised research solutions across diverse healthcare systems and patient populations is a key advantage. We ensure that each study is designed to align with regional healthcare infrastructure and regulatory landscapes.
Remote Monitoring Capabilities
Where applicable, we utilise advanced remote patient monitoring, telemedicine, and digital health tools to facilitate patient participation and data collection, regardless of location. This enhances accessibility and improves trial efficiency.