Timothy Joseph Lansangan
About Timothy Joseph Lansangan
Timothy Joseph Lansangan is a Senior Clinical Project Manager at Mirum Pharmaceuticals, with extensive experience in clinical research and drug development across various companies in the pharmaceutical industry. He holds a Master of Science in Clinical Research from the University of Liverpool and a Bachelor of Science in Pharmacy from the University of the Philippines.
Current Role at Mirum Pharmaceuticals
Timothy Joseph Lansangan serves as a Senior Clinical Project Manager at Mirum Pharmaceuticals. He has held this position since 2019, contributing to the company's clinical development efforts in Foster City, California. His role involves overseeing clinical trials and ensuring compliance with regulatory standards.
Previous Experience in Clinical Project Management
Lansangan has extensive experience in clinical project management. He worked at Novo Nordisk as a Clinical Project Manager from 2010 to 2014 and as an International Trial Manager from 2014 to 2016. His tenure at Grünenthal Group as a Global Operations Study Leader lasted from 2016 to 2017. Additionally, he was a Clinical Development Project Manager at Polyphor Ltd from 2018 to 2019.
Educational Background and Qualifications
Timothy Joseph Lansangan holds a Master of Science in Clinical Research from the University of Liverpool, which he completed from 2013 to 2015. He also earned a Bachelor of Science in Pharmacy from the University of the Philippines, studying there from 1999 to 2003. His educational background supports his expertise in the pharmaceutical industry.
Expertise in Pharmaceutical Industry
Lansangan possesses expertise in policy and Standard Operating Procedure (SOP) writing within the pharmaceutical sector. He has a strong background in drug and device development, which is supported by his various roles in clinical research and regulatory affairs throughout his career.
Career History in Regulatory Affairs
Lansangan has held positions in regulatory affairs, including his role as a Medical and Regulatory Affairs Analyst at Hospira from 2004 to 2006 and as a Medical and Regulatory Affairs Assistant at Pfizer for five months in 2003. These positions contributed to his understanding of regulatory compliance and drug development processes.