Daizy Moumi

Associate Director, Clinical Operations | London, England, United Kingdom

Professional Overview

Daizy Moumi is an experienced clinical operations professional with a proven track record in driving the successful execution of global clinical trials. As the Associate Director of Clinical Operations at Complement Therapeutics, she leverages her expertise in project management, regulatory affairs, and biospecimen management to optimize clinical study operations and ensure the timely delivery of quality data.

Experience Summary

Current Role

As the Associate Director of Clinical Operations at Complement Therapeutics, Daizy is responsible for leading cross-functional teams in the planning, implementation, and oversight of clinical studies. She collaborates closely with stakeholders to develop and execute strategies that enhance operational efficiency, mitigate risks, and maintain compliance with regulatory requirements. Daizy's strong leadership and problem-solving skills have been instrumental in driving the successful completion of critical clinical milestones for the organization.

Career Progression

Prior to her current role, Daizy held positions of increasing responsibility within the pharmaceutical and biotechnology industry. She served as a Senior Global Trial Manager at Novartis, where she managed the execution of complex multinational clinical trials. As an Associate Clinical Project Manager at Gyroscope Therapeutics, she played a key role in the development and implementation of innovative gene therapy protocols. Daizy's diverse experience also includes roles as a Clinical Site Manager at Janssen, a Clinical Trial Manager at UCL, and a Regulatory Affairs Associate at UNICANCER, where she demonstrated her versatility in navigating various aspects of clinical operations.

Academic Background

Daizy holds a Master's degree in Biomedical Sciences from King's College London, where she specialized in clinical research and data management. Her academic achievements, combined with her extensive practical experience, have equipped her with a comprehensive understanding of the pharmaceutical industry and a strong commitment to evidence-based decision-making.

Areas of Expertise

• Clinical trial management and operational oversight

• Regulatory affairs and compliance

• Biospecimen management and biobanking

• Cross-functional team leadership and collaboration

• Risk mitigation and operational optimization

• Stakeholder engagement and communication

Professional Impact

Daizy's contributions have been instrumental in the successful execution of multiple global clinical trials, leading to the advancement of innovative therapies and the improvement of patient outcomes. Her expertise in navigating complex regulatory frameworks and her ability to foster collaborative working relationships have been highly valued by her industry peers.

Conclusion

With her extensive experience, proven leadership skills, and deep understanding of the clinical operations landscape, Daizy Moumi is well-positioned to continue driving the success of Complement Therapeutics' clinical initiatives. Her commitment to excellence and her passion for advancing the field of clinical research make her a valuable asset to her organization and the pharmaceutical industry as a whole.