Executive Vice President Quality Assurance, TFS-Lund
Alistair has been working in clinical trials since1989 in a number of different roles. Alistair is TFS Director of Quality Assurance and Training at where he has setup and developed the Quality Assurance and Training department. He has held numerous training sessions in many different areas including audits, GCP, the European Directive, monitoring etc.
Fernando García de Blas Crespo
Project Director, TFS-Madrid
Fernando has been working in Clinical Trials and Non-Interventional studies since 2004, starting in Data Management and thereafter as CRA and PL in Clinical Operations. His main experience is in Oncology and he has a degree in Chemistry and a Masters in Technology and Management of the Chemical and Pharmaceutical Industry.
Lecturer, Sanders Communication
Rhiannon Sanders has a broad background in life sciences starting with 10 years in cancer research (PhD), followed by 10 years in the diagnostics industry. She has held positions from project leader to line manager to director of business development. After a further five years working with education issues and entrepreneurship for biotechnology,
Rhiannon started her own company in 2007 to teach advanced presentation technique for leaders, specialists and for challenging situations.
Associate Director Drug Safety, TFS-Lund
Margareta has an MSc in Pharmacy. She has worked in various positions at AstraZeneca for many years and she is well-experienced in pharmacovigilance/adverse event reporting. She is today responsible for pharmacovigilance, in post-marketing as well as in clinical studies
Associate Director, Medical Writing, TFS-Stockholm
Catherine has a PhD in Biochemistry and has been working as a Medical Writer for four years. Prior to this, she worked as a research scientist at AstraZeneca’s biotechnology laboratory and at the Department of Oral and Dental Science at the University of Bristol.
Senior Quality Assurance Manager, TFS-UK
Marc gained his PhD, in the hormonal control of seasonal breeding in 1985. The same year he started to work in the pharmaceutical industry. His experience includes 3 years in preclinical development performing drug assays and pharmacokinetic analyses. Since 1990 he has worked in clinical development as a study monitor and then as an international study manager in both France and the UK as a member of multinational teams in several therapeutic areas. He also has experience in continuous process improvement, writing and reviewing SOPs, international clinical operations and currently works as an auditor performing GxP audits. Marc is fluent in French and has a diploma in medical statistics awarded by the University of Paris.
Theo van Delft
Senior Quality Assurance Manager, TFS-Netherlands
Theo has been working in the clinical trial industry since 1998, first as a Quality Officer and later in various positions (Manager QA, Manager Clinical Research, Trainer, Project Manager and Consultant). Since 1984 Theo was working as consultant and trainer, manager, project manager and scientific researcher in different organizations and sectors.
Senior Director Project Management, TFS-Lund
Helene has been with TFS since September 2008 as a Unit Manager for Clinical Operations. Helene has been working in clinical trials as a Study Nurse, CRA, Project Leader since 1995. She has worked in Sweden, Denmark and Finland.
Medical Writer, TFS-Lund
Ulrika has a PhD in cardiovascular physiology. Before starting out as a Medical Writer two years ago, she was a researcher at the Department of Physiology, University of Gothenburg. She has published 11 scientific articles. Ulrika is a member of the European Medical Writers Association, and currently enrolled in their Professional Development Program. She is also a lecturer at the medical faculty in Gothenburg.