Matt McKendrick

Bio:

Matt is a results-driven leader specializing in Good Clinical Practice (GCP) and Trial Master File (TMF) excellence within clinical trials. As the Manager of GCP Excellence in Clinical Trials at Takeda, Matt ensures inspection readiness, TMF quality, and risk mitigation across the study lifecycle. He collaborates with cross-functional teams, mentors junior staff, and contributes to the development of global GCP processes to achieve the highest standards of compliance, reflecting his dedication to clinical quality and operational efficiency.

With nearly a decade of progressive experience in GCP and TMF operations, Matt has cultivated expertise in document management, regulatory compliance, and project oversight. His prior roles provided a strong foundation in TMF setup, quality control, and cross-functional coordination, enabling him to lead with precision and foresight.

Proficient in multiple eTMF systems, Matt leverages his technical acumen to uphold rigorous standards of TMF compliance, readiness, and inspection success. His ability to blend technical skills with a strategic mindset ensures optimal operational outcomes throughout clinical studies.

Matt’s commitment to excellence, paired with his collaborative and detail-oriented approach, positions him as an influential and trusted professional in the ever-evolving domain of clinical trial management.