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    Quality Manager

    With a Degree in Health Sciences from the University of Barcelona (2002, Spain), Duna initiated her career in Clinical Research after her Master in Clinical Trial Coordination at the Faculty of Medicine of the Hospital Clínic of Barcelona. Additionally, Duna went on to earn a Master in Management of Research & Development of European Projects at IDEC.

    As a Clinical Research Associate (CRA) at the Hospital Sant Pau, Duna was involved in clinical trials in Hematology, Rheumatology and Psychiatry. Since 2003, she has assumed multiples roles in a CRO, as a CRA, Head of the Communications Department, and as Project Manager in clinical trials and medical marketing projects. Duna also had the opportunity to collaborate in the development of Clinical Practice Guidelines for the treatment of follicular lymphoma.

    She has managed clinical trials from phases I to IV and studies for several pharmaceutical companies such as Bayer, Eisai, Ferrer, Grifols, Isdin, Novartis, Pfizer, Roche, Sanofi-Aventis, Amgen, Astra-Zeneca, and Eli Lilly.

    From 2012 to 2015, Duna held the position of Project Manager of clinical trials at MedSIR. She currently is applying her knowledge of Psychology in the role of People Manager within MedSIR’s Human Resources Department as well as collaborating with the Quality Assurance Department.

    Duna is fluent in Catalan, Spanish, and English.



    Quality Expert from iCROM

    With a degree in Biology and a postgraduate specialization Course in Quality Systems in the Pharmaceutical Industry and Research, I started being involved in clinical research in Nov 1996. After several years working as CRA in COPD, infectious diseases, cardiology and transplant clinical trials, I had the opportunity to become the head of the Oncology clinical trials office at Hospital Vall d’Hebron. Currently at i-CROM since Feb 2012, providing Quality services to MedSIR ARO.



    Quality Assurance Consultant

    With a Ph.D. in Philosophy in Bioethics from the University of Barcelona (2005), and with two Master’s Degrees: one in Bioethics and Law (1998), and another one in Clinical Trials (2006), Salvador has broad experience in clinical monitoring, site management, compliance assessment, mentoring, training and oversight programs for Clinical Research Associates.

    He has worked as a Clinical Research Associate on several international studies and has been responsible for overall site management for more than 6 years and Training and Development Management for over 3 years. He also has acquired experience in Risk Assessments and Auditing as a Quality Assurance Auditor. Salvador joined MedSIR in June 2017 as International Trial Lead.

    As Independent Expert for the European Commission, Salvador has been involved in evaluating proposals, reporting, and formulating recommendations as Ethics Expert since 2014.

    As a Bioethicist and Clinical Ethics Consultant, Salvador has been a teacher in several courses for both academic and non- academic institutions, offering lessons and conferences. During his period as Research Assistant at the University of Barcelona he had the opportunity to stay at the Zentrum für medizinische Ethik at the Ruhr-Universität (Bochum, Germany), and at the Center for Clinical Bioethics at Georgetown University (Washington DC, United States), as well as an author of publications related to Bioethics. Salvador is a member of the International Society for Clinical Bioethics.

    Salvador speaks Catalan, Spanish, English fluently and he also has knowledge of French and German.

MedSIR is always looking to add talented individuals to its team in a number of roles. If you are interested in getting us to know you better, please visit our Careers page to submit your CV to us.

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