ClinTec's Regional Manager for Germany, Austria and Switzerland has been with the company since 1999 and in this time has successfully Project-Managed numerous clinical trials across phases I – III in therapeutic areas such as Dermatology, Immunology, Rheumatology, Oncology and Cardiology. In addition to being responsible for all local regulatory submissions, he also manages a team of regional CRAs.

Before joining ClinTec, he worked for Baxter Deutschland as a Project Leader and Production Manager before moving into the field of Clinical Research. His experience in this field includes positions in Medical Writing, including an ad hoc position as a reviewer for two international Immunology Journals.

A graduate of L. Maximilians University with a Degree in Anthropology and Human Genetics, he completed a Master’s Thesis on Immunology at the Institute of Immunology, Munich before embarking on 4 years of research into HIV and completing a PhD in Immunology at the University of Munich.

ClinTec's Country Manager for France has 16 years of experience in the pharmaceutical industry, incorporating 11 years in international clinical trials in positions such as Senior CRA and Project Manager, monitoring sites in France, Belgium, Italy, Spain and Portugal. In addition to experience in clinical trials from Phases II-IV, she has worked as a Consultant for Strategic Analysis, Inc. focusing on business intelligence projects for the pharmaceutical industry.

After taking up positions within international companies in both clinical and business development roles, she joined ClinTec and has been instrumental in expanding our operations throughout France.

With an M.A in International Relations from the Johns Hopkins University, Washington, D.C. and Bologna, Italy, she obtained a D.E.A from La Sorbonne in Paris France before carrying out doctoral studies in Economics.

ClinTec’s Regional Director for Western and Northern Europe has over 18 years of experience in clinical research and has been with ClinTec since 2006. During this time, she has been responsible for building and developing the team in the Benelux region, in addition to taking the clinical monitoring lead in a global infertility study involving 12 countries over 3 continents – Australia, South America and Europe.

Trained as a medical microbiology analyst, she moved into clinical research as a Medical Representative and has since been involved in Phase II-IV trials across a broad range of therapeutic areas, including Anaesthesia, Pain Management, Cardiovascular disease, Endocrinology & Metabolism, Oncology and Rheumatology.

ClinTec's Regional Manager in Northern Europe and the Baltic States holds a strong background in Project Management; including managing a variety of full service projects and has experience in all aspects of drug and device development from pre-clinical to clinical trials, registration and marketing.

Having qualified as a Registered Nurse, she worked in internal medicine and cardiology for 8 years, before moving onto a career as a Research Nurse and Lecturer in heart diseases. She holds over 10 years of experience in clinical research with Investigator-initiated studies, Global Pharma companies, Medtech and Local Biotech companies.

Recent successes at ClinTec include the management of a suite of key global studies covering almost 20 countries across Europe, Africa, Latin America and Asia as well as local full service projects. Additionally, she has conducted successful feasibility studies and patient enrollment & retention projects.

Our Regional Manager for Spain and Portugal has over 16 years experience within the clinical research arena across a diverse range of therapeutic areas in phases I – IV. She has extensive experience of preparing and coordinating the applications and approvals to Regulatory Authorities at both a national and international level.

Her previous experience before joining ClinTec includes working for Global CROs in both Project Management and Regulatory Affairs positions. She was also a Clinical Research Manager for a CRO in Spain with overall responsibility for leading local and international clinical projects.

Having graduated in University Autonoma of Barcelona with a Bachelors Degree in Biochemistry, she worked at Yale University, USA, before moving into clinical research. She has also undertaken further training in Pharmacovigilance, Project Management, GCP and GLP.

ClinTec’s Country Manager in Italy has been with ClinTec since November 2010 and in responsible for managing all operations across the country. With over 10 years of experience in the pharmaceutical industry, he has worked in the full drug development process and has extensive experience across Phase II-IV.

Before joining ClinTec, he gained experience with international CROs and is well versed in EU and US regulations and has worked across a range of therapeutic areas including Gastroenterology, Cardiology, Infectious Diseases, Neurology and Oncology.  He has extensive knowledge of Medical Device regulations and experience in project management, patient recruitment strategies and nutritional products trials.

He is a graduate of University La Sapienza with a master degree in Chemistry, attended several training as Clinical Project Manager and currently holds four professional memberships: SSFA (Italian Pharmaceutical Scientific Society); SSFA Medical Devices Working Group; Assomonitor (Italian Association of Monitors) and TOPRA (The Organisation for Professionals in Regulatory Affairs).