Martina Kollmann
About Martina Kollmann
Martina Kollmann is a Senior Clinical Trial Manager at Bristol-Myers Squibb with extensive experience in managing clinical trials from Phase I to Phase IV.
Current Position at Bristol-Myers Squibb
Martina Kollmann currently holds the position of Senior Clinical Trial Manager at Bristol-Myers Squibb. Based in München, she also serves as a Senior Clinical Site Manager, demonstrating her multifaceted expertise within the company. Her responsibilities include overseeing multiple clinical trial sites, ensuring compliance with regulatory requirements, and coordinating between various stakeholders to ensure the smooth operation of clinical trials.
Previous Experience at MSD Sharp & Dohme GmbH
Before joining Bristol-Myers Squibb, Martina Kollmann worked as a Clinical Project Manager at MSD Sharp & Dohme GmbH from 2009 to 2014. Located in München und Umgebung, Deutschland, she handled various aspects of clinical trials, from planning to execution. Her role involved coordinating with clinical sites, managing project timelines, and ensuring data integrity throughout the study's course.
Role at Essex Pharma GmbH
Martina Kollmann's career also includes significant tenures at Essex Pharma GmbH. From 2003 to 2008, she served as a Clinical Research Associate, where she conducted quality control visits, audits, and inspections. Earlier, from 2000 to 2002, she was a Medical Field Manager, where she managed clinical operations on the ground, ensuring that trials ran smoothly and efficiently.
Educational Background at Technische Universität München-Weihenstephan
Martina Kollmann studied at Technische Universität München-Weihenstephan, where she earned a Diplom Ökotrophologe (Dipl.oec.troph). She completed her studies from 1993 to 1999, acquiring a strong foundation in nutrition science which has been instrumental in her subsequent roles in clinical trial management.
Clinical Trial Management Expertise
With extensive experience managing clinical trials from Phase I to Phase IV, Martina Kollmann's expertise includes site selection, database lock, and overseeing national investigator meetings. She is adept at supervising Contract Research Organizations (CROs) and has substantial experience in quality control visits, audits, and inspections. She also manages Investigator-Initiated Trials (IITs) and contributes to the creation of study documents, ensuring thorough preparation and execution of clinical trials.