Career Options in the Pharmaceutical and Biomedical Industry

Part 1: Setting the scene.- Chapter 1: Life after Academia: Launching your Pharma/Biotech Career.- Chapter 2: Competences for Pharmacists.- Chapter 3: Job and Career Opportunities in the Pharmaceutical Industry: An Overview.- Part 2: Opportunities along the drug/product life cycle.- Chapter 4: Career Opportunities in Toxicology.- Chapter 5: Job Possibilities in Clinical Research.- Chapter 6: How to Get and Develop a Career in a Market Access Role in the Medical Devices Industry.- Chapter 7: Job Opportunities in Pharmaceutical Marketing.- Chapter 8: Working in Medical Affairs and Clinical Operations: Life-Changing Careers.- Chapter 9: The Role of Medical Science Liaison.- Chapter 10: Career Development for Physicians in the Biopharmaceutical Industry.- Part 3: Opportunities in Supportive Functions.- Chapter 11: Job and Career Opportunities in Regulatory Affairs/Science.- Chapter 12: Job Opportunities in Clinical Research Quality Assurance.- Chapter 13: Job Opportunities in QualityAssurance Related to Manufacturing of Medicinal Products.- Part 4: Other Opportunities in the Pharmaceutical and Biomedical Sector.- Chapter 14: Careers Perspective in a Science and Technology Park.- Chapter 15: To be or not to be: Entrepreneurship and Enterprise Creation as a Way to Innovate in Life Sciences.- Chapter 16: How to Become a Successful Hospital and Community Pharmacist.- Part 5: Practical tips and tricks.- Chapter 17: A Successful Career in the Life Sciences Industry: How to Write your Strongest Resumé and Ace that Interview.- Chapter 18: Skill Building for Career Advancement: Public Speaking and Networking.- Chapter 19: Training Opportunities for a Career in the Pharmaceutical and Biomedical Industry/Sector.

Josse R. Thomas graduated as a Pharmacist and holds a postgraduate and a PhD degree in Medical Sciences (experimental and clinical pharmacology) from the University of Leuven, Belgium. He is certified as a Clinical Pharmacologist and has more than 30 years of experience in clinical drug development in the pharmaceutical industry. In addition, he held or holds various academic and consulting positions, including former Visiting Professor at KU Leuven (clinical drug development), former member of the Medical Research Ethics Committee of UZ/KU Leuven, member of the Clinical Trials Board of the Belgian Health Care Knowledge Centre (KCE), National Expert participating in the European Commission DG SANTE Union Controls within the framework of the Clinical Trials Regulation (CTR), and Senior Consultant at PharmaCS. He is also co-author of the book 'Global New Drug Development: An Introduction', published by Wiley-Blackwell, and a reference in its field.

Prof. Luciano Saso (Faculty of Pharmacy and Medicine, Sapienza University of Rome, Italy) is author of more than 350 scientific articles published in peer reviewed international journals (H-index Google Scholar 58, Scopus 48). He coordinated several research projects and has been referee for many national and international funding agencies and international scientific journals in the last 30 years.  Prof. Saso has extensive experience in international relations and he has been Deputy -Rector at Sapienza University of Rome in the last 7 years. In the last 20 years, he participated in several projects and has been speaker and chair at many international conferences organised by the UNICA network of the universities from the Capitals of Europe (http://www.unica-network.eu/) and other university associations. Prof. Saso is currently President of UNICA (2015-2023) and Member of the Steering Committee of CIVIS