Kia Thomsen Email & Phone Number

My background is BSc in Engineering (Chemistry) supplied with GCP and GMP-courses and theexam as “Lægemiddelkonsulent”. I have experience within setting up, running and archivingclinical studies (phase I-IV) from both a pharmaceutical company (Novo Nordisk), a CRO company(Parexel), and my current position at a clinical trial site (Clinical Research Unit, Oncology, Herlev Hospital).I find it exciting supporting the execution of clinical trials, contributing to the best solution for eachproject, assuring timely deliverables and valid data. My approach is structured, proactive, with ahigh quality mind-set and a can-do attitude. I am experienced in assuring properupload, coordination, indexing, and quality control of trial documents in different IT systems.I am familiar with medical terminology and used to navigating in clinical trial protocols, contractsand clinical trial documentation. In my current position at a clinical trial site, I am involved in thestart-up, running and archiving of approximately 30 trials annually. I perform QC and databaseupload of trial documents, keep track of contracts, and act as an anchor of competence for tasks inSundhedsplatformen related to research. Furthermore, I deal with trial supplies, arrange meetingsand training sessions and write minutes. My colleagues appreciate, that I have an eye on the detailscombined with an analytical approach to issues, striving for the smartest solutions seen in a holisticview. A natural thing for me is to act as a mentor for less experienced colleagues and to do so in a respectful way.I believe I can contribute in a positive way to your company since I like to stay curious, identifyareas of concern, and follow things through. I have flair for IT, am detail oriented and have a strongquality mind-set. I work dedicatedly and enjoy supporting various stakeholders and knowing theirway of work. It motivates me to collaborate with people of different professions and responsibilitiesand to ensure alignment of expectations and deliveries throughout the whole process. It is importantfor me to work for inspection readiness by assuring compliance with GXP and other regulatoryrequirements, specifications, and SOPs.Last but not least, it is important for me to have fun while working.

Listed skills include Clinical Trials, Clinical Research, Pharmaceutical Industry, Gmp, and 14 others.